US20230201806A1 - Catalyst composition, hydrocarbon partial oxidizer, and fuel cell system - Google Patents

Catalyst composition, hydrocarbon partial oxidizer, and fuel cell system Download PDF

Info

Publication number
US20230201806A1
US20230201806A1 US18/087,920 US202218087920A US2023201806A1 US 20230201806 A1 US20230201806 A1 US 20230201806A1 US 202218087920 A US202218087920 A US 202218087920A US 2023201806 A1 US2023201806 A1 US 2023201806A1
Authority
US
United States
Prior art keywords
catalyst composition
oxide
mass
alumina
hydrocarbon
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Abandoned
Application number
US18/087,920
Inventor
Jun Sawada
Wataru Ishii
Daisuke Kurashina
Hiroki Homma
Takamitsu Kino
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Honda Motor Co Ltd
Mitsui Mining and Smelting Co Ltd
Original Assignee
Honda Motor Co Ltd
Mitsui Mining and Smelting Co Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Honda Motor Co Ltd, Mitsui Mining and Smelting Co Ltd filed Critical Honda Motor Co Ltd
Assigned to MITSUI MINING & SMELTING CO., LTD., HONDA MOTOR CO., LTD. reassignment MITSUI MINING & SMELTING CO., LTD. ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: HOMMA, HIROKI, KINO, TAKAMITSU, SAWADA, JUN, KURASHINA, DAISUKE, ISHII, WATARU
Publication of US20230201806A1 publication Critical patent/US20230201806A1/en
Abandoned legal-status Critical Current

Links

Images

Classifications

    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J23/00—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00
    • B01J23/38—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of noble metals
    • B01J23/54—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of noble metals combined with metals, oxides or hydroxides provided for in groups B01J23/02 - B01J23/36
    • B01J23/56—Platinum group metals
    • B01J23/63—Platinum group metals with rare earths or actinides
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J21/00—Catalysts comprising the elements, oxides, or hydroxides of magnesium, boron, aluminium, carbon, silicon, titanium, zirconium, or hafnium
    • B01J21/02—Boron or aluminium; Oxides or hydroxides thereof
    • B01J21/04—Alumina
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J21/00—Catalysts comprising the elements, oxides, or hydroxides of magnesium, boron, aluminium, carbon, silicon, titanium, zirconium, or hafnium
    • B01J21/06—Silicon, titanium, zirconium or hafnium; Oxides or hydroxides thereof
    • B01J21/066—Zirconium or hafnium; Oxides or hydroxides thereof
    • B01J35/0006—
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J35/00—Catalysts, in general, characterised by their form or physical properties
    • B01J35/19—Catalysts containing parts with different compositions
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J35/00—Catalysts, in general, characterised by their form or physical properties
    • B01J35/30—Catalysts, in general, characterised by their form or physical properties characterised by their physical properties
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J35/00—Catalysts, in general, characterised by their form or physical properties
    • B01J35/30—Catalysts, in general, characterised by their form or physical properties characterised by their physical properties
    • B01J35/31—Density
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J35/00—Catalysts, in general, characterised by their form or physical properties
    • B01J35/40—Catalysts, in general, characterised by their form or physical properties characterised by dimensions, e.g. grain size
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J35/00—Catalysts, in general, characterised by their form or physical properties
    • B01J35/60—Catalysts, in general, characterised by their form or physical properties characterised by their surface properties or porosity
    • B01J35/61—Surface area
    • B01J35/612—Surface area less than 10 m2/g
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J35/00—Catalysts, in general, characterised by their form or physical properties
    • B01J35/60—Catalysts, in general, characterised by their form or physical properties characterised by their surface properties or porosity
    • B01J35/61—Surface area
    • B01J35/615—100-500 m2/g
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J35/00—Catalysts, in general, characterised by their form or physical properties
    • B01J35/60—Catalysts, in general, characterised by their form or physical properties characterised by their surface properties or porosity
    • B01J35/63—Pore volume
    • B01J35/633—Pore volume less than 0.5 ml/g
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J37/00—Processes, in general, for preparing catalysts; Processes, in general, for activation of catalysts
    • B01J37/02—Impregnation, coating or precipitation
    • B01J37/0201—Impregnation
    • C—CHEMISTRY; METALLURGY
    • C01—INORGANIC CHEMISTRY
    • C01B—NON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
    • C01B3/00—Hydrogen; Gaseous mixtures containing hydrogen; Separation of hydrogen from mixtures containing it; Purification of hydrogen
    • C01B3/02—Production of hydrogen or of gaseous mixtures containing a substantial proportion of hydrogen
    • C01B3/22—Production of hydrogen or of gaseous mixtures containing a substantial proportion of hydrogen by decomposition of gaseous or liquid organic compounds
    • C01B3/24—Production of hydrogen or of gaseous mixtures containing a substantial proportion of hydrogen by decomposition of gaseous or liquid organic compounds of hydrocarbons
    • C01B3/26—Production of hydrogen or of gaseous mixtures containing a substantial proportion of hydrogen by decomposition of gaseous or liquid organic compounds of hydrocarbons using catalysts
    • C—CHEMISTRY; METALLURGY
    • C01—INORGANIC CHEMISTRY
    • C01B—NON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
    • C01B3/00—Hydrogen; Gaseous mixtures containing hydrogen; Separation of hydrogen from mixtures containing it; Purification of hydrogen
    • C01B3/02—Production of hydrogen or of gaseous mixtures containing a substantial proportion of hydrogen
    • C01B3/32—Production of hydrogen or of gaseous mixtures containing a substantial proportion of hydrogen by reaction of gaseous or liquid organic compounds with gasifying agents, e.g. water, carbon dioxide, air
    • C01B3/34—Production of hydrogen or of gaseous mixtures containing a substantial proportion of hydrogen by reaction of gaseous or liquid organic compounds with gasifying agents, e.g. water, carbon dioxide, air by reaction of hydrocarbons with gasifying agents
    • C01B3/38—Production of hydrogen or of gaseous mixtures containing a substantial proportion of hydrogen by reaction of gaseous or liquid organic compounds with gasifying agents, e.g. water, carbon dioxide, air by reaction of hydrocarbons with gasifying agents using catalysts
    • C01B3/386—Catalytic partial combustion
    • C—CHEMISTRY; METALLURGY
    • C01—INORGANIC CHEMISTRY
    • C01B—NON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
    • C01B3/00—Hydrogen; Gaseous mixtures containing hydrogen; Separation of hydrogen from mixtures containing it; Purification of hydrogen
    • C01B3/02—Production of hydrogen or of gaseous mixtures containing a substantial proportion of hydrogen
    • C01B3/32—Production of hydrogen or of gaseous mixtures containing a substantial proportion of hydrogen by reaction of gaseous or liquid organic compounds with gasifying agents, e.g. water, carbon dioxide, air
    • C01B3/34—Production of hydrogen or of gaseous mixtures containing a substantial proportion of hydrogen by reaction of gaseous or liquid organic compounds with gasifying agents, e.g. water, carbon dioxide, air by reaction of hydrocarbons with gasifying agents
    • C01B3/38—Production of hydrogen or of gaseous mixtures containing a substantial proportion of hydrogen by reaction of gaseous or liquid organic compounds with gasifying agents, e.g. water, carbon dioxide, air by reaction of hydrocarbons with gasifying agents using catalysts
    • C01B3/40—Production of hydrogen or of gaseous mixtures containing a substantial proportion of hydrogen by reaction of gaseous or liquid organic compounds with gasifying agents, e.g. water, carbon dioxide, air by reaction of hydrocarbons with gasifying agents using catalysts characterised by the catalyst
    • C—CHEMISTRY; METALLURGY
    • C01—INORGANIC CHEMISTRY
    • C01B—NON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
    • C01B32/00—Carbon; Compounds thereof
    • C01B32/40—Carbon monoxide
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M8/00—Fuel cells; Manufacture thereof
    • H01M8/06—Combination of fuel cells with means for production of reactants or for treatment of residues
    • H01M8/0606—Combination of fuel cells with means for production of reactants or for treatment of residues with means for production of gaseous reactants
    • H01M8/0612—Combination of fuel cells with means for production of reactants or for treatment of residues with means for production of gaseous reactants from carbon-containing material
    • H01M8/0618—Reforming processes, e.g. autothermal, partial oxidation or steam reforming
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M8/00—Fuel cells; Manufacture thereof
    • H01M8/06—Combination of fuel cells with means for production of reactants or for treatment of residues
    • H01M8/0606—Combination of fuel cells with means for production of reactants or for treatment of residues with means for production of gaseous reactants
    • H01M8/0612—Combination of fuel cells with means for production of reactants or for treatment of residues with means for production of gaseous reactants from carbon-containing material
    • H01M8/0625—Combination of fuel cells with means for production of reactants or for treatment of residues with means for production of gaseous reactants from carbon-containing material in a modular combined reactor/fuel cell structure
    • H01M8/0631—Reactor construction specially adapted for combination reactor/fuel cell
    • C—CHEMISTRY; METALLURGY
    • C01—INORGANIC CHEMISTRY
    • C01B—NON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
    • C01B2203/00—Integrated processes for the production of hydrogen or synthesis gas
    • C01B2203/02—Processes for making hydrogen or synthesis gas
    • C01B2203/0205—Processes for making hydrogen or synthesis gas containing a reforming step
    • C01B2203/0227—Processes for making hydrogen or synthesis gas containing a reforming step containing a catalytic reforming step
    • C01B2203/0233—Processes for making hydrogen or synthesis gas containing a reforming step containing a catalytic reforming step the reforming step being a steam reforming step
    • C—CHEMISTRY; METALLURGY
    • C01—INORGANIC CHEMISTRY
    • C01B—NON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
    • C01B2203/00—Integrated processes for the production of hydrogen or synthesis gas
    • C01B2203/02—Processes for making hydrogen or synthesis gas
    • C01B2203/025—Processes for making hydrogen or synthesis gas containing a partial oxidation step
    • C01B2203/0261—Processes for making hydrogen or synthesis gas containing a partial oxidation step containing a catalytic partial oxidation step [CPO]
    • C—CHEMISTRY; METALLURGY
    • C01—INORGANIC CHEMISTRY
    • C01B—NON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
    • C01B2203/00—Integrated processes for the production of hydrogen or synthesis gas
    • C01B2203/02—Processes for making hydrogen or synthesis gas
    • C01B2203/0283—Processes for making hydrogen or synthesis gas containing a CO-shift step, i.e. a water gas shift step
    • C—CHEMISTRY; METALLURGY
    • C01—INORGANIC CHEMISTRY
    • C01B—NON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
    • C01B2203/00—Integrated processes for the production of hydrogen or synthesis gas
    • C01B2203/06—Integration with other chemical processes
    • C—CHEMISTRY; METALLURGY
    • C01—INORGANIC CHEMISTRY
    • C01B—NON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
    • C01B2203/00—Integrated processes for the production of hydrogen or synthesis gas
    • C01B2203/06—Integration with other chemical processes
    • C01B2203/066—Integration with other chemical processes with fuel cells
    • C—CHEMISTRY; METALLURGY
    • C01—INORGANIC CHEMISTRY
    • C01B—NON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
    • C01B2203/00—Integrated processes for the production of hydrogen or synthesis gas
    • C01B2203/08—Methods of heating or cooling
    • C01B2203/0805—Methods of heating the process for making hydrogen or synthesis gas
    • C01B2203/085—Methods of heating the process for making hydrogen or synthesis gas by electric heating
    • C—CHEMISTRY; METALLURGY
    • C01—INORGANIC CHEMISTRY
    • C01B—NON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
    • C01B2203/00—Integrated processes for the production of hydrogen or synthesis gas
    • C01B2203/10—Catalysts for performing the hydrogen forming reactions
    • C01B2203/1041—Composition of the catalyst
    • C01B2203/1047—Group VIII metal catalysts
    • C01B2203/1064—Platinum group metal catalysts
    • C—CHEMISTRY; METALLURGY
    • C01—INORGANIC CHEMISTRY
    • C01B—NON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
    • C01B2203/00—Integrated processes for the production of hydrogen or synthesis gas
    • C01B2203/10—Catalysts for performing the hydrogen forming reactions
    • C01B2203/1041—Composition of the catalyst
    • C01B2203/1047—Group VIII metal catalysts
    • C01B2203/1064—Platinum group metal catalysts
    • C01B2203/107—Platinum catalysts
    • C—CHEMISTRY; METALLURGY
    • C01—INORGANIC CHEMISTRY
    • C01B—NON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
    • C01B2203/00—Integrated processes for the production of hydrogen or synthesis gas
    • C01B2203/10—Catalysts for performing the hydrogen forming reactions
    • C01B2203/1041—Composition of the catalyst
    • C01B2203/1082—Composition of support materials
    • C—CHEMISTRY; METALLURGY
    • C01—INORGANIC CHEMISTRY
    • C01B—NON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
    • C01B2203/00—Integrated processes for the production of hydrogen or synthesis gas
    • C01B2203/12—Feeding the process for making hydrogen or synthesis gas
    • C01B2203/1205—Composition of the feed
    • C01B2203/1211—Organic compounds or organic mixtures used in the process for making hydrogen or synthesis gas
    • C01B2203/1235—Hydrocarbons
    • C—CHEMISTRY; METALLURGY
    • C01—INORGANIC CHEMISTRY
    • C01B—NON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
    • C01B2203/00—Integrated processes for the production of hydrogen or synthesis gas
    • C01B2203/12—Feeding the process for making hydrogen or synthesis gas
    • C01B2203/1205—Composition of the feed
    • C01B2203/1211—Organic compounds or organic mixtures used in the process for making hydrogen or synthesis gas
    • C01B2203/1235—Hydrocarbons
    • C01B2203/1241—Natural gas or methane
    • C—CHEMISTRY; METALLURGY
    • C01—INORGANIC CHEMISTRY
    • C01B—NON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
    • C01B2203/00—Integrated processes for the production of hydrogen or synthesis gas
    • C01B2203/12—Feeding the process for making hydrogen or synthesis gas
    • C01B2203/1205—Composition of the feed
    • C01B2203/1211—Organic compounds or organic mixtures used in the process for making hydrogen or synthesis gas
    • C01B2203/1235—Hydrocarbons
    • C01B2203/1247—Higher hydrocarbons
    • C—CHEMISTRY; METALLURGY
    • C01—INORGANIC CHEMISTRY
    • C01B—NON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
    • C01B2203/00—Integrated processes for the production of hydrogen or synthesis gas
    • C01B2203/12—Feeding the process for making hydrogen or synthesis gas
    • C01B2203/1258—Pre-treatment of the feed
    • C01B2203/1264—Catalytic pre-treatment of the feed
    • C01B2203/127—Catalytic desulfurisation
    • C—CHEMISTRY; METALLURGY
    • C01—INORGANIC CHEMISTRY
    • C01B—NON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
    • C01B3/00—Hydrogen; Gaseous mixtures containing hydrogen; Separation of hydrogen from mixtures containing it; Purification of hydrogen
    • C01B3/02—Production of hydrogen or of gaseous mixtures containing a substantial proportion of hydrogen
    • C01B3/32—Production of hydrogen or of gaseous mixtures containing a substantial proportion of hydrogen by reaction of gaseous or liquid organic compounds with gasifying agents, e.g. water, carbon dioxide, air
    • C01B3/34—Production of hydrogen or of gaseous mixtures containing a substantial proportion of hydrogen by reaction of gaseous or liquid organic compounds with gasifying agents, e.g. water, carbon dioxide, air by reaction of hydrocarbons with gasifying agents
    • C01B3/38—Production of hydrogen or of gaseous mixtures containing a substantial proportion of hydrogen by reaction of gaseous or liquid organic compounds with gasifying agents, e.g. water, carbon dioxide, air by reaction of hydrocarbons with gasifying agents using catalysts
    • C01B3/382—Multi-step processes
    • C—CHEMISTRY; METALLURGY
    • C01—INORGANIC CHEMISTRY
    • C01B—NON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
    • C01B3/00—Hydrogen; Gaseous mixtures containing hydrogen; Separation of hydrogen from mixtures containing it; Purification of hydrogen
    • C01B3/02—Production of hydrogen or of gaseous mixtures containing a substantial proportion of hydrogen
    • C01B3/32—Production of hydrogen or of gaseous mixtures containing a substantial proportion of hydrogen by reaction of gaseous or liquid organic compounds with gasifying agents, e.g. water, carbon dioxide, air
    • C01B3/34—Production of hydrogen or of gaseous mixtures containing a substantial proportion of hydrogen by reaction of gaseous or liquid organic compounds with gasifying agents, e.g. water, carbon dioxide, air by reaction of hydrocarbons with gasifying agents
    • C01B3/48—Production of hydrogen or of gaseous mixtures containing a substantial proportion of hydrogen by reaction of gaseous or liquid organic compounds with gasifying agents, e.g. water, carbon dioxide, air by reaction of hydrocarbons with gasifying agents followed by reaction of water vapour with carbon monoxide
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02E—REDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
    • Y02E60/00—Enabling technologies; Technologies with a potential or indirect contribution to GHG emissions mitigation
    • Y02E60/30—Hydrogen technology
    • Y02E60/50—Fuel cells

Definitions

  • the present invention relates to a catalyst composition that partially oxidizes a hydrocarbon to produce hydrogen and carbon monoxide, a hydrocarbon partial oxidizer including the catalyst composition, and a fuel cell system including the hydrocarbon partial oxidizer.
  • hydrogen is produced from a hydrocarbon through a partial oxidation reaction, a steam reforming reaction, and a water-gas shift reaction, and electric power is generated by a fuel cell using the produced hydrogen.
  • a catalyst composition for the steam reforming reaction there are known, for example, a catalyst composition in which a platinum group element and a Ce oxide are supported on an alumina carrier (e.g., an ⁇ -alumina carrier)
  • Patent Literature 1 Japanese Patent Laid-Open No. 2011-088066
  • Patent Literature 2 Japanese Patent Laid-Open No. 2000-178007
  • Patent Literature 3 Japanese Translation of PCT International Application Publication No. 2004-507425.
  • the catalyst composition that partially oxidizes a hydrocarbon to produce hydrogen and carbon monoxide produces hydrogen and carbon monoxide through the partial oxidation reaction of the hydrocarbon. Since this reaction is an exothermic reaction, the catalyst composition is exposed to a high temperature over an extended period. Therefore, the catalyst composition is required to have improved heat resistance.
  • a conventional catalyst composition is exposed to a high temperature, its catalytic activity is likely to deteriorate.
  • the catalyst composition described in Patent Literatures 1 and 2 are exposed to high temperatures, there is a risk that sintering of the Ce oxide and sintering of the platinum group element associated with the sintering of the Ce oxide and/or embedding of the platinum group element may occur, resulting in a decrease in catalytic activity.
  • the ⁇ -alumina used as a carrier in the catalyst composition described in Patent Literature 3 has a large initial specific surface area, which is advantageous for surface enrichment of supported components, while it also has such a property that its specific surface area changes greatly upon exposure to a high temperature.
  • high temperature means a temperature of 200° C. or higher (especially, 300° C. or higher).
  • an object of the present invention is to provide: a catalyst composition that partially oxidizes a hydrocarbon to produce hydrogen and carbon monoxide, the catalytic activity of which is unlikely to deteriorate even when the catalyst composition is exposed to a high temperature; a hydrocarbon partial oxidizer including the catalyst composition; and a fuel cell system including the hydrocarbon partial oxidizer.
  • the present invention provides the following inventions.
  • a catalyst composition that partially oxidizes a hydrocarbon to produce hydrogen and carbon monoxide, the catalyst composition comprising: a carrier that comprises ⁇ -alumina; and supported components that are supported on the carrier,
  • the supported components comprise at least one platinum group element, a Ce oxide, and a Zr oxide.
  • the present invention provides: a catalyst composition that partially oxidizes a hydrocarbon to produce hydrogen and carbon monoxide, the catalytic activity of which is unlikely to deteriorate even when the catalyst composition is exposed to a high temperature; a hydrocarbon partial oxidizer including the catalyst composition; and a fuel cell system including the hydrocarbon partial oxidizer.
  • FIG. 1 is a schematic view of a fuel cell system according to one embodiment of the present invention.
  • FIG. 2 is a schematic view of an evaluating device used in Test Example 1.
  • the catalyst composition of the present invention is described below.
  • the form of the catalyst composition of the present invention is, for example, an aggregate of particles (powder form).
  • the catalyst composition of the present invention may be formed into a desired shape such as a pellet or a layer.
  • the catalyst composition of the present invention is a catalyst composition that partially oxidizes a hydrocarbon to produce hydrogen and carbon monoxide.
  • Conditions of the partial oxidation reaction are not particularly limited as long as the partial oxidation reaction can proceed.
  • the temperature is preferably 100° C. or higher and 1,000° C. or lower, more preferably 200° C. or higher and 800° C. or lower, and even more preferably 300° C. or higher and 700° C. or lower.
  • the number of carbon atoms of the hydrocarbon is not particularly limited, and is, for example, 1 or more and 40 or less, preferably 1 or more and 30 or less, and more preferably 1 or more and 20 or less.
  • the hydrocarbon include saturated aliphatic hydrocarbons, unsaturated aliphatic hydrocarbons, and aromatic hydrocarbons.
  • the saturated aliphatic hydrocarbons and unsaturated aliphatic hydrocarbons may be chain-like or cyclic. The chain may be linear or branched.
  • the aromatic hydrocarbons may be monocyclic or polycyclic.
  • hydrocarbon examples include chain saturated aliphatic hydrocarbons such as methane, ethane, propane, butane, pentane, hexane, heptane, octane, nonane, decane, dodecane, tridecane, tetradecane, pentadecane, hexadecane, heptadecane, octadecane, nonadecane, and eicosane; alicyclic hydrocarbons such as cyclopentane and cyclohexane; unsaturated aliphatic hydrocarbons such as ethylene, propylene, butene, pentene, and hexene; and aromatic hydrocarbons such as benzene, toluene, xylene, and naphthalene.
  • chain saturated aliphatic hydrocarbons such as methane, ethane, propane, butane, pentane, hexane,
  • the hydrocarbon may have one or more substituents.
  • substituents include halogen atoms (e.g., F, Cl, Br, and I), hydroxy groups, alkoxy groups, carboxyl groups, ester groups, aldehyde groups, and acyl groups.
  • the hydrocarbon to be partially oxidized by the catalyst composition of the present invention may be a mixture of two or more hydrocarbons.
  • the catalyst compositions of the present invention contain a carrier.
  • the carrier is, for example, particulate.
  • the particulate shape includes, for example, spherical (e.g., truly spherical and ellipsoidal), acicular, scaly (flaky), columnar (e.g., cylindrical and prismatic), and other shapes.
  • the carrier is spherical.
  • the carrier is preferably porous.
  • the carrier contains ⁇ -alumina.
  • the ⁇ -alumina contained in the carrier forms an ⁇ -alumina phase. Since the ⁇ -alumina has a small initial specific surface area, the supported components are easily supported deep into the pores of the carrier. In addition, the change in specific surface area of the ⁇ -alumina is small upon exposure to a high temperature, making the blockage of the pores of the carrier less likely to occur. Therefore, even when the catalyst composition of the present invention is exposed to a high temperature, a state in which the reaction gas easily reaches the supported components supported deep into the pores of the carrier is maintained, making the catalytic activity of the catalyst composition unlikely to deteriorate.
  • the carrier may contain components other than the ⁇ -alumina.
  • the components other than the ⁇ -alumina include alumina other than the ⁇ -alumina, silica, iron, and sodium.
  • alumina other than the ⁇ -alumina include ⁇ -alumina, ⁇ -alumina, ⁇ -alumina, and ⁇ -alumina.
  • the content of the ⁇ -alumina in the carrier is preferably 90% by mass or more, more preferably 95% by mass or more, even more preferably 98% by mass or more, based on the mass of the carrier.
  • the upper limit is 100% by mass.
  • the content of each element in the carrier can be measured by analyzing a sample obtained from the catalyst compositions of the present invention by energy dispersive X-ray spectroscopy (EDS) to obtain an element mapping, and performing EDS elemental analysis on designated particles in the obtained element mapping.
  • EDS energy dispersive X-ray spectroscopy
  • the content of each element in the designated particles can be measured by qualitatively identifying (color-coding) the carrier particles and other particles by elemental mapping and performing composition analysis (elemental analysis) on the designated particles.
  • the content of alumina in the carrier can be calculated as an amount of Al in terms of Al 2 O 3 , based on the content of Al in the carrier.
  • the crystal form of alumina in the carrier can be determined by X-ray diffraction (XRD).
  • the content of the carrier in the catalyst composition of the present invention can be appropriately adjusted. From the viewpoint of more effectively suppressing the deterioration of the catalytic activity of the catalyst composition of the present invention, the content of the carrier in the catalyst composition of the present invention is adjusted so that the content of ⁇ -alumina derived from the carrier is preferably 70% by mass or more and 95% by mass or less, more preferably 75% by mass or more and 95% by mass or less, and even more preferably 80% by mass or more and 95% by mass or less, based on the mass of catalyst composition of the present invention.
  • the content of ⁇ -alumina in the catalyst composition of the present invention can be calculated from the composition of the raw materials used in the production of the catalyst composition of the present invention.
  • the content of ⁇ -alumina in the catalyst composition of the present invention can be measured using a conventional method such as scanning electron microscopy-energy dispersive X-ray spectroscopy (SEM-EDX), X-ray fluorescence analysis (XRF), and inductively coupled plasma atomic emission spectrometry (ICP-AES). Specifically, the method is as follows.
  • a sample obtained from the catalyst composition of the present invention is analyzed by XRF or ICP-AES to identify 20 metal elements in descending order, from higher content to lower content.
  • the 20 identified metal elements include Al.
  • the sample is then analyzed by SEM-EDX.
  • SEM-EDX the 20 metal elements identified above are targeted for analysis.
  • the total mole % of the 20 metal elements is set to 100 mole % to analyze the mole % of each metal element.
  • the content of Al in the sample in terms of Al 2 O 3 is calculated from the average value of the mole % of Al in the 10 visual fields.
  • the crystal form of alumina in the sample can be determined by X-ray diffraction (XRD).
  • the catalyst composition of the present invention includes supported components supported on the carrier.
  • a component is supported on the carrier means a state in which the component is physically or chemically adsorbed or retained on the outer surfaces or inner surfaces of the pores of the carrier.
  • the fact that the component is supported on the carrier can be confirmed using, for example, a scanning electron microscope-energy dispersive X-ray analyzer (SEM-EDX). Specifically, in the elemental mapping obtained using SEM-EDX or the like, when the component and the carrier are present in the same region, it can be determined that the component is supported on the carrier.
  • SEM-EDX scanning electron microscope-energy dispersive X-ray analyzer
  • the supported components include at least one platinum group element, a Ce oxide, and a Zr oxide.
  • the catalyst composition of the present invention includes at least one platinum group element supported on the carrier, a Ce oxide supported on the carrier, and a Zr oxide supported on the carrier.
  • the platinum group element is a catalytically active component, while the Ce oxide and the Zr oxide are cocatalyst components.
  • the at least one platinum group element can be selected from the group of platinum group elements consisting of Pt, Pd, Rh, Ru, Os, and Ir. From the viewpoint of more effectively expressing catalytic activity, the at least one platinum group element preferably includes Pt and Rh.
  • the content of the platinum group element in terms of metal is preferably 0.1% by mass or more and 2.0% by mass or less, more preferably 0.3% by mass or more and 1.5% by mass or less, and even more preferably 0.5% by mass or more and 1.0% by mass or less, based on the mass of the catalyst composition of the present invention.
  • the term “the content of the platinum group element in terms of metal” means the content of one platinum group element in terms of metal if the catalyst composition of the present invention contains the one platinum group element, and the total content of two or more platinum group elements in terms of metal when the catalyst composition of the present invention contains the two or more platinum group elements.
  • the content of the platinum group element in the catalyst composition of the present invention can be calculated or measured in the same manner as the content of ⁇ -alumina in the catalyst composition of the present invention.
  • the platinum group element is supported on the carrier in a form capable of functioning as a catalytically-active component, for example, in the form of a metal composed of the platinum group element, an alloy containing the platinum group element, a compound containing the platinum group element (such as an oxide of the platinum group element), or the like.
  • the catalytically-active component is, for example, particulate.
  • the Ce oxide is composed of a Ce element and an O element.
  • a stoichiometric composition of the Ce oxide is represented by CeO 2
  • the Ce oxide may have a composition that deviates from the stoichiometric composition (non-stoichiometric composition).
  • the composition of the Ce oxide contained in the catalyst composition of the present invention may be stoichiometric composition or non-stoichiometric composition (e.g., CeO 1.8 and CeO 1.9 ).
  • the catalyst composition of the present invention may contain one type of Ce oxide, or two or more types of Ce oxides.
  • the Zr oxide is composed of a Zr element and an O element. Although a stoichiometric composition of the Zr oxide is represented by ZrO 2 , the Zr oxide may have a composition that deviates from the stoichiometric composition (non-stoichiometric composition).
  • the composition of the Zr oxide contained in the catalyst composition of the present invention may be stoichiometric composition or non-stoichiometric composition (e.g., ZrO 1.8 and ZrO 1.9 ).
  • the catalyst composition of the present invention may contain one type of Zr oxide, or two or more types of Zr oxides.
  • the Ce oxide and the Zr oxide are, for example, particulate.
  • the content of the Ce oxide in the catalyst composition of the present invention in terms of CeO 2 is preferably 8.5% by mass or more and 13.5% by mass or less, more preferably 9.0% by mass or more and 13.0% by mass or less, and even more preferably 9.5% by mass or more and 12.5% by mass or less, based on the mass of the catalyst composition of the present invention.
  • the content of the Ce oxide in terms of CeO 2 means the content of one Ce oxide in terms of CeO 2 when the catalyst composition of the present invention contains the one Ce oxide, and the total content of two or more Ce oxides in terms of CeO 2 when the catalyst composition of the present invention contains the two or more Ce oxides.
  • the content of the Ce oxide in the catalyst composition of the present invention in terms of CeO 2 can be calculated or measured in the same manner as the content of ⁇ -alumina in the catalyst composition of the present invention.
  • the content of the Zr oxide in the catalyst composition of the present invention in terms of ZrO 2 is preferably 0.3% by mass or more and 2.5% by mass or less, more preferably 0.4% by mass or more and 2.0% by mass or less, and even more preferably 0.5% by mass or more and 1.5% by mass or less, based on the mass of the catalyst composition of the present invention.
  • the content of the Zr oxide in terms of ZrO 2 means the content of one Zr oxide in terms of ZrO 2 when the catalyst composition of the present invention contains the one Zr oxide, and the total content of two or more Zr oxides in terms of ZrO 2 when the catalyst composition of the present invention contains the two or more Zr oxides.
  • the content of the Zr oxide in the catalyst composition of the present invention in terms of ZrO 2 can be calculated or measured in the same manner as the content of ⁇ -alumina in the catalyst composition of the present invention.
  • the ratio of the Ce oxide in terms of CeO 2 to the total content of the Ce oxide in terms of CeO 2 and the Zr oxide in terms of ZrO 2 is preferably 0.77 or more and 0.98 or less, more preferably 0.82 or more and 0.97 or less, and even more preferably 0.86 or more and 0.96 or less.
  • Ce—Zr composite oxide a composite oxide containing Ce and Zr, hereinafter referred to as “Ce—Zr composite oxide”.
  • the Ce—Zr composite oxide is, for example, particulate.
  • sintering of the Ce oxide and sintering of the platinum group element associated with the sintering of the Ce oxide and/or embedding of the platinum group element associated with the sintering of the Ce oxide are less likely to occur, compared to a case where the Ce oxide and the Zr oxide are present separately.
  • the sintering of the Ce oxide and the sintering of the platinum group element associated with the sintering of the Ce oxide and/or the embedding of the platinum group element associated with the sintering of the Ce oxide are more effectively suppressed, thus more effectively suppressing the deterioration of the catalytic activity of the catalyst composition of the present invention.
  • the entire Ce oxide may be present in the form of the Ce—Zr composite oxide, and the entire Zr oxide may be present in the form of the Ce—Zr composite oxide.
  • Ce, Zr, and O preferably form a solid solution phase.
  • Ce, Zr, and O may form a single phase (Ce oxide phase and/or Zr oxide phase), which is a crystalline phase or an amorphous phase.
  • XRD X-ray diffraction
  • the XRD pattern can be obtained by performing XRD with CuK ⁇ using a sample obtained from the catalyst composition of the present invention and a commercially available X-ray diffraction device. Specific XRD conditions are as mentioned in Examples.
  • the catalyst composition of the present invention may include one or more other supported components supported on the carrier.
  • other components include oxides of rare earth metal elements other than Ce (e.g., Nd, La, Y, and Pr) and oxides of alkaline earth metal elements (e.g., Mg, Ca, Sr, and Ba). These oxides are, for example, particulate. At least a part of these oxides may form a composite oxide with the Ce oxide and/or the Zr oxide.
  • the total content of such other supported components is preferably 5% by mass or less, more preferably 3% by mass or less, and even more preferably 1% by mass or less, based on the mass of the catalyst composition of the present invention.
  • the lower limit is zero.
  • the content of such other supported components in the catalyst composition of the present invention can be calculated or measured in the same manner as the content of ⁇ -alumina in the catalyst composition of the present invention.
  • the sum of the content of ⁇ -alumina derived from the carrier, the content of the Ce oxide supported on the carrier in terms of CeO 2 , and the content of the Zr oxide supported on the carrier in terms of ZrO 2 is preferably 98.0% by mass or more and 99.9% by mass or less, more preferably 98.5% by mass or more and 99.7% by mass or less, and even more preferably 99.0% by mass or more and 99.5% by mass or less, based on the mass of the catalyst composition of the present invention.
  • the catalyst composition of the present invention can be produced, for example, by mixing a solution containing a salt of a platinum group element, a solution containing a cerium salt, a solution containing a zirconium salt, and carrier particles each containing ⁇ -alumina, followed by drying and calcination.
  • the calcined product may be pulverized as necessary.
  • the salt of the platinum group element may be, for example, a nitrate, an ammine complex salt, a chloride or the like.
  • the cerium salt may be, for example, a nitrate, an acetate or the like.
  • the zirconium salt may be, for example, a nitrate, an acetate or the like.
  • the solvents contained in the solution containing the salt of the platinum group element, the solution containing the cerium salt, and the solution containing the zirconium salt are each, for example, water (such as ion exchanged water).
  • the solution containing the salt of the platinum group element, the solution containing the cerium salt, and the solution containing the zirconium salt may each contain an organic solvent such as alcohol.
  • the drying temperature is, for example, 70° C. or higher and 150° C. or lower.
  • the calcination temperature is, for example, 400° C. or higher and 700° C. or lower.
  • the calcination time is, for example, 1 hour or more and 10 hours or less. The calcination can be carried out, for example, in an air atmosphere.
  • the carrier particles each containing ⁇ -alumina used in the production of the catalyst composition of the present invention preferably have the following physical properties.
  • the BET specific surface area of the carrier particles is preferably 1 m 2 /g or more and 20 m 2 /g or less, and more preferably 2 m 2 /g or more and 10 m 2 /g or less.
  • the BET specific surface area is measured according to JIS R1626, “Measuring methods for the specific surface area of fine ceramic powders by gas adsorption using the BET method,” “6.2 Flow method,” “(3.5) Single-point method.”
  • a nitrogen-helium gas mixture containing 30% by volume of nitrogen as an adsorption gas and 70% by volume of helium as a carrier gas is used as a gas.
  • BELSORP-MR6 manufactured by MicrotracBEL Corp. is used as a measurement device.
  • the pore volume (total pore volume in the range of a pore diameter of 3 nm or more and 500 ⁇ m or less) of the carrier particles is preferably 0.3 cm 3 /g or more and 0.6 cm 3 /g or less, and more preferably 0.4 cm 3 /g or more and 0.5 cm 3 /g or less.
  • the pore volume is measured by mercury porosimetry using a mercury porosimeter.
  • the mercury porosimetry is performed in accordance with JIS R 1655:2003.
  • AutoPore IV 9520 manufactured by SHIMADZU CORPORATION, is used as a measuring device.
  • the average particle size of the carrier particles is preferably 1.0 mm or more and 5.0 mm or less, and more preferably 2.0 mm or more and 4.0 mm or less.
  • a method of measuring the average particle size of the carrier particles is as follows.
  • the carrier particles are observed using an optical microscope, and unidirectional particle diameters (Feret diameters) of 100 carrier particles arbitrarily selected from the visual field are measured to define an average value as the average particle size of the carrier particles.
  • the packing density (tap density) of the carrier particles is preferably 0.70 g/cm 3 or more and 1.00 g/cm 3 or less, and more preferably 0.80 g/cm 3 or more and 0.90 g/cm 3 or less.
  • a method of measuring the packing density (tap density) of the carrier particles is as follows. 30 g of carrier particles is put in a 150-ml glass measuring cylinder and tapped 350 times in a stroke of 60 mm with a shaking specific gravity meter (KRS-409, manufactured by Kuramochi Kagaku Kikai Seisakusho K.K), and then the packing density (tap density) is measured.
  • KRS-409 shaking specific gravity meter
  • a fuel cell system 100 according to one embodiment of the invention is described below based on FIG. 1 .
  • Two or more of embodiments described below can be used in combination, and the combination of two or more embodiments is also encompassed by the present invention.
  • a fuel cell system 100 can be used for various applications, including stationary as well as automotive use and the like.
  • the fuel cell system 100 includes a processing unit 110 and a control unit 111 that controls operation of the processing unit 110 .
  • the control unit 111 is, for example, a computer and includes a main control unit and a storage unit.
  • the main control unit is, for example, a CPU (central processing unit), and controls the operation of the processing unit 110 by reading and executing programs, data, and the like stored in the storage unit.
  • the storage unit is composed of, for example, a RAM (Random Access Memory), a ROM (Read Only Memory), a hard disk, or other storage devices, and stores programs, data, and the like that control processes executed by the processing unit 110 .
  • the processing unit 110 in the fuel cell system 100 includes a hydrocarbon partial oxidizer 12 , a fuel cell 16 , a raw material supplying unit 17 , and an oxidant gas supplying unit 19 .
  • the processing unit 110 in the fuel cell system 100 may optionally include a mixer 13 , a steam reformer 14 , a shift reactor 15 , and a steam supplying unit 18 .
  • the raw material supplying unit 17 supplies a raw material gas G 1 containing a hydrocarbon to the hydrocarbon partial oxidizer 12 .
  • the raw material gas G 1 includes one or more hydrocarbon-containing materials selected from, for example, city gas, natural gas, LPG, naphtha, gasoline, kerosene, and light oil.
  • the raw material gas G 1 may contain hydrogen, water, carbon dioxide, carbon monoxide, nitrogen, oxygen, and the like.
  • the raw material gas G 1 contains air.
  • the air may be mixed with a hydrocarbon in the raw material supplying unit 17 , or may be mixed with the hydrocarbon on the way that the hydrocarbon is supplied from the raw material supplying unit 17 to the hydrocarbon partial oxidizer 12 .
  • the raw material supplying unit 17 includes a tank for storing the raw material gas G 1 , a supply pipe for supplying the raw material gas G 1 in the tank to the hydrocarbon partial oxidizer 12 , and a pump provided in the supply pipe, and supplies the raw material gas G 1 in the tank to the hydrocarbon partial oxidizer 12 through the supply pipe by using sucking and discharging forces of the pump.
  • the raw material supplying unit 17 may include a desulfurizer for desulfurizing the raw material gas G 1 .
  • the desulfurizer includes a container and a desulfurizing agent contained within the container.
  • the desulfurizing agent a known agent can be used.
  • the O 2 /C (ratio of the molar amount of oxygen molecules to the molar amount of carbon atoms contained in the hydrocarbon) in the raw material gas G 1 can be appropriately set depending on a desired yield of hydrogen, characteristics of the fuel cell system, reaction conditions, and the like.
  • the hydrocarbon partial oxidizer 12 includes the catalyst composition of the present invention.
  • the hydrocarbon partial oxidizer 12 includes a container and the catalyst composition of the invention contained within the container.
  • the raw material gas G 1 supplied to the hydrocarbon partial oxidizer 12 is brought into contact with the catalyst composition of the present invention, and a hydrocarbon in the raw material gas G 1 is partially oxidized to produce a reformed gas G 2 containing hydrogen and carbon monoxide.
  • Conditions of the partial oxidation reaction in the hydrocarbon partial oxidizer 12 are not particularly limited as long as the partial oxidation reaction can proceed.
  • the temperature is preferably 100° C. or higher and 1,000° C. or lower, more preferably 200° C. or higher and 800° C. or lower, and even more preferably 300° C. or higher and 700° C. or lower.
  • the reformed gas G 2 produced in the hydrocarbon partial oxidizer 12 is supplied to the fuel cell 16 .
  • the reformed gas G 2 is supplied to an anode electrode 161 side of the fuel cell 16 .
  • the fuel cell 16 generates electric power by electrochemical reaction between hydrogen in the reformed gas G 2 and oxygen in an oxidant gas R supplied by the oxidant gas supplying unit 19 .
  • a mixer 13 may be provided.
  • the reformed gas G 2 produced in the hydrocarbon partial oxidizer 12 is supplied to the mixer 13 .
  • a steam supplying unit 18 may be provided.
  • the steam supplying unit 18 supplies steam W to the mixer 13 .
  • the steam supplying unit 18 may include a steam generating unit for generating the steam W from water.
  • the steam supplying unit 18 includes a tank for storing the steam W, a supply pipe for supplying the steam in the tank to the mixer 13 , and a pump provided in the supply pipe, and supplies the steam W in the tank to the mixer 13 through the supply pipe by using sucking and discharging forces of the pump.
  • the reformed gas G 2 and the steam W are mixed to generate a mixed gas G 3 containing the reformed gas G 2 and the steam W.
  • the generated mixed gas G 3 is supplied to the steam reformer 14 .
  • the steam reformer 14 may be provided.
  • the steam reformer 14 includes a catalyst composition for steam reforming reaction.
  • the steam reformer 14 includes a container and the catalyst composition for steam reforming reaction contained within the container.
  • the catalyst composition for the steam reforming reaction a known composition can be used.
  • the mixed gas G 3 supplied to the steam reformer 14 is brought into contact with the catalyst composition for steam reforming reaction, and a hydrocarbon in the mixed gas G 3 is steam-reformed to produce a reformed gas G 4 containing hydrogen and carbon monoxide.
  • the reformed gas G 4 produced in the steam reformer 14 is supplied to the fuel cell 16 .
  • the reformed gas G 4 is supplied to an anode electrode 161 side of the fuel cell 16 .
  • the fuel cell 16 generates electric power by electrochemical reaction between hydrogen in the reformed gas G 4 and oxygen in an oxidant gas R supplied by the oxidant gas supplying unit 19 .
  • a shift reactor 15 may be provided.
  • the shift reactor 15 includes a catalyst composition for water-gas shift reaction.
  • the shift reactor 15 includes a container and the catalyst composition for water-gas shift reaction contained within the container.
  • the catalyst composition for water-gas shift reaction a known composition can be used.
  • the reformed gas G 4 supplied to the shift reactor 15 is brought into contact with the catalyst composition for water-gas shift reaction, and carbon monoxide and steam in the reformed gas G 4 react to produce a fuel gas G 5 containing hydrogen and carbon dioxide.
  • the water-gas shift reaction is represented by the following equation.
  • the fuel gas G 5 produced in the shift reactor 15 is supplied to the fuel cell 16 .
  • the fuel gas G 5 is supplied to the anode electrode 161 side of the fuel cell 16 .
  • the fuel cell 16 generates electric power by electrochemical reaction between hydrogen in the fuel gas G 5 and oxygen in an oxidant gas R supplied by the oxidant gas supplying unit 19 .
  • the oxidant gas supplying unit 19 supplies an oxidant gas R to the fuel cell 16 .
  • the oxidant gas R is, for example, air.
  • the oxidant gas R is supplied to a cathode electrode 162 side of the fuel cell 16 .
  • the oxidant gas supplying unit 19 includes a tank for storing the oxidant gas R, a supply pipe for supplying the oxidant gas R in the tank to the fuel cell 16 , and a pump provided in the supply pipe, and supplies the oxidant gas R in the tank to the fuel cell 16 through the supply pipe by using sucking and discharging forces of the pump.
  • the fuel cell 16 a known fuel cell can be used.
  • the fuel cell 16 is, for example, a solid oxide fuel cell (SOFC).
  • SOFC solid oxide fuel cell
  • a plurality of fuel cells 16 may be laminated to form a fuel cell stack.
  • the fuel cell 16 is, for example, an electrolyte/electrode assembly (MEA) in which the anode electrode 161 and the cathode electrode 162 are respectively provided on one surface and the other surface of an electrolyte 163 composed of an oxide ion conductor such as stabilized zirconia.
  • MEA electrolyte/electrode assembly
  • a reaction proceeds in which hydrogen reacts with oxide ions to form water and release electrons, while at the cathode electrode 162 , a reaction proceeds in which oxygen gains electrons to become oxide ions.
  • An electric load (not shown) may be connected electrically to the anode electrode 161 and the cathode electrode 162 .
  • spherical ⁇ -alumina pellets (specific surface area: about 4 m 2 /g, pore volume: about 0.43 cm 3 /g, packing density: about 0.86 g/cm 3 , average particle size: about 2.5 mm) were allowed to stand and dried for 5 hours to give dried alumina pellets.
  • a platinum nitrate solution and a rhodium nitrate solution were each weighed so that the sum of the content of Pt in terms of metal and the content of Rh in terms of metal was 0.5% by mass or more and 1.0% by mass or less, based on the mass of the final product, Pt—Rh-ceria-zirconia-supporting calcined alumina pellet.
  • a cerium nitrate solution and a zirconium nitrate solution were each weighed so that the content of the Ce oxide in terms of CeO 2 and the content of the Zr oxide in terms of ZrO 2 were as shown in Table 1, based on the mass of the final product, Pt—Rh-ceria-zirconia-supporting calcined alumina pellet.
  • the solutions were mixed and stirred for 10 minutes to give a mixed solution.
  • the obtained mixed solution was charged into the dried alumina pellets and stirred for 10 minutes to allow the alumina pellets to absorb the mixed solution.
  • the content of the dried alumina pellets charged was adjusted so that the content of solid matter of the alumina pellets absorbed with the mixed solution was 100 g in total.
  • the alumina pellets having absorbed the mixed solution were dried under an environment of 120° C. until no weight change was observed to give Pt—Rh-cerium-zirconium-supporting dried alumina pellets.
  • the obtained Pt—Rh-cerium-zirconium-supporting dried alumina pellets were calcined at 500° C. for 3 hours to give Pt—Rh-ceria-zirconia-supporting calcined alumina pellets.
  • the composition of the obtained Pt—Rh-ceria-zirconia-supporting calcined alumina pellets is shown in Table 1. Note that in Table 1, “% by mass” in Example 1 is based on the mass of the Pt—Rh-ceria-zirconia-supporting calcined alumina pellet.
  • XRD X-ray diffraction
  • the platinum nitrate solution and the rhodium nitrate solution were weighed so that the content (% by mass) of Pt in terms of metal and the content (% by mass) of Rh in terms of metal were each the same as in Example 1, based on the mass of the final product, Pt—Rh-ceria-supporting calcined alumina pellet.
  • the cerium nitrate solution was weighed so that the content of the Ce oxide in terms of CeO 2 was as shown in Table 1, based on the mass of the final product, Pt—Rh-ceria-supporting calcined alumina pellet.
  • Example 2 The same operation as in Example 1 was carried out to give Pt—Rh-cerium-supporting dried alumina pellets, except that the solutions were mixed and stirred for 10 minutes and a mixed solution was obtained (a zirconium nitrate solution was not used).
  • the obtained Pt—Rh-cerium-supporting dried alumina pellets were calcined at 500° C. for 3 hours to give Pt—Rh-ceria-supporting calcined alumina pellets.
  • the composition of the obtained Pt—Rh-ceria-supporting calcined alumina pellets is shown in Table 1. Note that in Table 1, “% by mass” in Comparative Example 1 is based on the mass of the Pt—Rh-ceria-supporting calcined alumina pellet.
  • XRD X-ray diffraction
  • Example 2 The same operation as in Example 1 was carried out to give Pt—Rh-cerium-zirconium-supporting dried alumina pellets, except that under an environment of 120° C., 100 g of spherical ⁇ -alumina pellets (specific surface area: about 210 m 2 /g, pore volume: about 0.43 cm 3 /g, packing density: about 0.85 g/cm 3 , average particle size: about 2.5 mm) were allowed to stand and dried for 5 hours, and dried alumina pellets were obtained.
  • 100 g of spherical ⁇ -alumina pellets (specific surface area: about 210 m 2 /g, pore volume: about 0.43 cm 3 /g, packing density: about 0.85 g/cm 3 , average particle size: about 2.5 mm) were allowed to stand and dried for 5 hours, and dried alumina pellets were obtained.
  • XRD X-ray diffraction
  • the Pt—Rh-ceria-zirconia-supporting calcined alumina pellets obtained in Example 1 were installed in a tubular furnace, and a simulated fuel gas containing air and hydrocarbon was circulated.
  • a simulated fuel gas containing air and hydrocarbon was circulated.
  • the ratio of the molar amount of oxygen molecules derived from the air to the molar amount of carbon atoms derived from the hydrocarbon (O 2 /C ratio) was adjusted to be 0.5.
  • the temperature of the tubular furnace was increased to 1,000° C. at a temperature increasing rate of 5° C./min while the simulated fuel gas was circulated, and the Pt—Rh-ceria-zirconia-supporting calcined alumina pellets obtained in Example 1 were treated at 1,000° C. for 24 hours to prepare an aging-treated sample.
  • the evaluation device illustrated in FIG. 2 was used to measure the ignition temperature of the aging-treated samples.
  • the flow rates of fuel gas (city gas) supplied from a cylinder 1 and air supplied from a cylinder 3 are adjusted by a gas mass flow controller 2 and a gas mass flow controller 4 , respectively.
  • the fuel gas supplied from the cylinder 1 and the air supplied from the cylinder 3 are mixed in a mixing unit 5 and transferred to a partial oxidation catalyst 7 contained within a stainless steel container in an electric furnace 6 , and the gas partially oxidized by the partial oxidation catalyst 7 is discharged through a bubbler 8 .
  • a partial oxidation catalyst 7 contained within a stainless steel container in an electric furnace 6
  • the gas partially oxidized by the partial oxidation catalyst 7 is discharged through a bubbler 8 . Note that each of the aging-treated samples obtained in (1) above were used as the partial oxidation catalyst 7 .
  • the ignition temperature and the temperature after heating were measured according to the following procedure. Note that the amount of the partial oxidation catalyst 7 in the stainless steel container in the electric furnace 6 was adjusted to a volume of 1.5 cm 3 , and the flow rates of the fuel gas and air supplied to the partial oxidation catalyst 7 were adjusted so that the space velocity (SV) divided by the catalyst volume was about 30,000 h ⁇ 1 , and the ratio of the molar amount of oxygen molecules in the supplied air to the molar amount of carbon atoms in the supplied fuel gas (O 2 /C ratio) was 0.5.
  • SV space velocity
  • thermocouple 9 The temperature of the electric furnace was increased until the temperature of the furnace, as measured by a thermocouple 9 , reached 200° C.
  • thermocouple 10 The setting temperature of the electric furnace was increased by 10° C., the temperature of the partial oxidation catalyst 7 was measured by a thermocouple 10 , and the temperature of an inlet gas was measured by a thermocouple 11 located in front of the partial oxidation catalyst 7 .
  • Example 2 Ignition Temperature after temperature (° C.) heating (° C.) Example 1 500 590 Comparative 535 600 Example 1 Comparative 585 610 Example 2
  • Example 1 In the aging-treated sample of Example 1, even when exposed to a high temperature, a state in which the reaction gas easily reaches the supported components supported deep into the pores of the carrier was maintained by using ⁇ -alumina as the carrier. Furthermore, because of the inclusion of the Zr oxide, the effects of preventing the sintering of the platinum group element associated with the sintering of the Ce oxide and/or the embedding of the platinum group element associated with the sintering of the Ce oxide were preferably exhibited. As a result, the activity of the catalyst did not decrease, the state in which the partial oxidation reaction easily occurred was maintained, and showed the low ignition temperature.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Organic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Inorganic Chemistry (AREA)
  • General Chemical & Material Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Manufacturing & Machinery (AREA)
  • Sustainable Development (AREA)
  • Sustainable Energy (AREA)
  • Electrochemistry (AREA)
  • Combustion & Propulsion (AREA)
  • General Health & Medical Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Catalysts (AREA)
  • Fuel Cell (AREA)
  • Hydrogen, Water And Hydrids (AREA)

Abstract

An object of the present invention is to provide a catalyst composition that partially oxidizes a hydrocarbon to produce hydrogen and carbon monoxide, the catalytic activity of which is unlikely to deteriorate even when the catalyst composition is exposed to a high temperature, and the present invention provides a catalyst composition that partially oxidizes a hydrocarbon to produce hydrogen and carbon monoxide, including: a carrier that contains α-alumina; and a supported components that are supported on the carrier, wherein the supported components includes at least one platinum group element, a Ce oxide, and a Zr oxide.

Description

    CROSS-REFERENCE TO RELATED APPLICATIONS
  • The present application is based upon and claims the benefit of priority from Japanese Patent Application No. 2021-211477, filed Dec. 24, 2021; the entire contents of which are incorporated herein by reference.
    • BACKGROUND OF THE INVENTION Field of the Invention
  • The present invention relates to a catalyst composition that partially oxidizes a hydrocarbon to produce hydrogen and carbon monoxide, a hydrocarbon partial oxidizer including the catalyst composition, and a fuel cell system including the hydrocarbon partial oxidizer.
    • Background Art
  • In order to reduce environmental loads, spreading of fuel cell systems has been promoted in recent years, and fuel cell systems for household have also been developed.
  • In a fuel cell system, for example, hydrogen is produced from a hydrocarbon through a partial oxidation reaction, a steam reforming reaction, and a water-gas shift reaction, and electric power is generated by a fuel cell using the produced hydrogen.
  • When the hydrocarbon is CH4, the partial oxidation reaction, the steam reforming reaction, and the water-gas shift reaction are represented by the following equations.

  • Partial oxidation reaction: CH4+½O2→2H2+CO

  • Steam reforming reaction: CH4+H2O→3H2+CO

  • Water-gas shift reaction: CO+H2O→H2+CO2
  • As a catalyst composition for the steam reforming reaction, there are known, for example, a catalyst composition in which a platinum group element and a Ce oxide are supported on an alumina carrier (e.g., an α-alumina carrier) (Patent Literature 1: Japanese Patent Laid-Open No. 2011-088066; and Patent Literature 2: Japanese Patent Laid-Open No. 2000-178007), and a catalyst composition in which a platinum group element, a Ce oxide, and a Zr oxide are supported on a γ-alumina carrier (Patent Literature 3: Japanese Translation of PCT International Application Publication No. 2004-507425).
    • SUMMARY OF THE INVENTION
  • The catalyst composition that partially oxidizes a hydrocarbon to produce hydrogen and carbon monoxide produces hydrogen and carbon monoxide through the partial oxidation reaction of the hydrocarbon. Since this reaction is an exothermic reaction, the catalyst composition is exposed to a high temperature over an extended period. Therefore, the catalyst composition is required to have improved heat resistance. However, when a conventional catalyst composition is exposed to a high temperature, its catalytic activity is likely to deteriorate. For example, when the catalyst composition described in Patent Literatures 1 and 2 are exposed to high temperatures, there is a risk that sintering of the Ce oxide and sintering of the platinum group element associated with the sintering of the Ce oxide and/or embedding of the platinum group element may occur, resulting in a decrease in catalytic activity. The γ-alumina used as a carrier in the catalyst composition described in Patent Literature 3 has a large initial specific surface area, which is advantageous for surface enrichment of supported components, while it also has such a property that its specific surface area changes greatly upon exposure to a high temperature. Thus, when the catalyst composition described in Patent Literature 3 is exposed to a high temperature, there is a risk that not only the embedding of the platinum group element supported on the outer surface of the γ-alumina but also blockage of pores of the γ-alumina may occur and thus cause a reaction gas to hardly reach the supported components, resulting in a decrease in catalytic activity. Note that the term “high temperature” as used herein means a temperature of 200° C. or higher (especially, 300° C. or higher).
  • Therefore, an object of the present invention is to provide: a catalyst composition that partially oxidizes a hydrocarbon to produce hydrogen and carbon monoxide, the catalytic activity of which is unlikely to deteriorate even when the catalyst composition is exposed to a high temperature; a hydrocarbon partial oxidizer including the catalyst composition; and a fuel cell system including the hydrocarbon partial oxidizer.
  • In order to solve the above problems, the present invention provides the following inventions.
  • [1] A catalyst composition that partially oxidizes a hydrocarbon to produce hydrogen and carbon monoxide, the catalyst composition comprising: a carrier that comprises α-alumina; and supported components that are supported on the carrier,
  • wherein the supported components comprise at least one platinum group element, a Ce oxide, and a Zr oxide.
  • [2] The catalyst composition according to [1], wherein a content of the α-alumina is 70% by mass or more and 95% by mass or less, based on a mass of the catalyst composition.
    [3] The catalyst composition according to [1] or [2], wherein a content of the Ce oxide in terms of CeO2 is 8.5% by mass or more and 13.5% by mass or less, based on a mass of the catalyst composition.
    [4] The catalyst composition according to any one of [1] to [3], wherein a content of the Zr oxide in terms of ZrO2 is 0.3% by mass or more and 2.5% by mass or less, based on a mass of the catalyst composition.
    [5] The catalyst composition according to any one of [1] to [4], wherein at least a part of the Ce oxide and at least a part of the Zr oxide are present in a form of a composite oxide.
    [6] The catalyst composition according to [5], wherein in an X-ray diffraction pattern, at least one of peaks derived from the Ce oxide has a peak top at 20=47.61° to 49°.
    [7] The catalyst composition according to any one of [1] to [6], wherein the at least one platinum group element comprises Pt and Rh.
    [8] A hydrocarbon partial oxidizer that partially oxidizes a hydrocarbon to produce hydrogen and carbon monoxide, the hydrocarbon partial oxidizer comprising the catalyst composition according to any one of [1] to [7].
    [9] A fuel cell system comprising: the hydrocarbon partial oxidizer according to [8]; and a fuel cell that generates electric power by a reaction between the hydrogen produced in the hydrocarbon partial oxidizer and an oxidant gas.
  • The present invention provides: a catalyst composition that partially oxidizes a hydrocarbon to produce hydrogen and carbon monoxide, the catalytic activity of which is unlikely to deteriorate even when the catalyst composition is exposed to a high temperature; a hydrocarbon partial oxidizer including the catalyst composition; and a fuel cell system including the hydrocarbon partial oxidizer.
    • BRIEF DESCRIPTION OF THE DRAWINGS
  • FIG. 1 is a schematic view of a fuel cell system according to one embodiment of the present invention; and
  • FIG. 2 is a schematic view of an evaluating device used in Test Example 1.
    •  DETAILED DESCRIPTION OF THE INVENTION <<Catalyst Composition>>
  • The catalyst composition of the present invention is described below.
  • The form of the catalyst composition of the present invention is, for example, an aggregate of particles (powder form). The catalyst composition of the present invention may be formed into a desired shape such as a pellet or a layer.
  • The catalyst composition of the present invention is a catalyst composition that partially oxidizes a hydrocarbon to produce hydrogen and carbon monoxide.
  • When the hydrocarbon is CnHm, the partial oxidation reaction is represented by the following equation.

  • Partial oxidation reaction: CnHm +n/2O2 →m/2H2 +nCO
  • Conditions of the partial oxidation reaction are not particularly limited as long as the partial oxidation reaction can proceed. The temperature is preferably 100° C. or higher and 1,000° C. or lower, more preferably 200° C. or higher and 800° C. or lower, and even more preferably 300° C. or higher and 700° C. or lower.
  • The number of carbon atoms of the hydrocarbon is not particularly limited, and is, for example, 1 or more and 40 or less, preferably 1 or more and 30 or less, and more preferably 1 or more and 20 or less. Examples of the hydrocarbon include saturated aliphatic hydrocarbons, unsaturated aliphatic hydrocarbons, and aromatic hydrocarbons. The saturated aliphatic hydrocarbons and unsaturated aliphatic hydrocarbons may be chain-like or cyclic. The chain may be linear or branched. The aromatic hydrocarbons may be monocyclic or polycyclic.
  • Specific examples of the hydrocarbon include chain saturated aliphatic hydrocarbons such as methane, ethane, propane, butane, pentane, hexane, heptane, octane, nonane, decane, dodecane, tridecane, tetradecane, pentadecane, hexadecane, heptadecane, octadecane, nonadecane, and eicosane; alicyclic hydrocarbons such as cyclopentane and cyclohexane; unsaturated aliphatic hydrocarbons such as ethylene, propylene, butene, pentene, and hexene; and aromatic hydrocarbons such as benzene, toluene, xylene, and naphthalene. The hydrocarbon may have one or more substituents. Examples of the substituents include halogen atoms (e.g., F, Cl, Br, and I), hydroxy groups, alkoxy groups, carboxyl groups, ester groups, aldehyde groups, and acyl groups.
  • The hydrocarbon to be partially oxidized by the catalyst composition of the present invention may be a mixture of two or more hydrocarbons.
    • <Carrier>
  • The catalyst compositions of the present invention contain a carrier.
  • The carrier is, for example, particulate. The particulate shape includes, for example, spherical (e.g., truly spherical and ellipsoidal), acicular, scaly (flaky), columnar (e.g., cylindrical and prismatic), and other shapes. In one embodiment, the carrier is spherical.
  • From the viewpoint of improving supporting properties of supported components, the carrier is preferably porous.
  • The carrier contains α-alumina. The α-alumina contained in the carrier forms an α-alumina phase. Since the α-alumina has a small initial specific surface area, the supported components are easily supported deep into the pores of the carrier. In addition, the change in specific surface area of the α-alumina is small upon exposure to a high temperature, making the blockage of the pores of the carrier less likely to occur. Therefore, even when the catalyst composition of the present invention is exposed to a high temperature, a state in which the reaction gas easily reaches the supported components supported deep into the pores of the carrier is maintained, making the catalytic activity of the catalyst composition unlikely to deteriorate.
  • The carrier may contain components other than the α-alumina. Examples of the components other than the α-alumina include alumina other than the α-alumina, silica, iron, and sodium. Examples of alumina other than the α-alumina include γ-alumina, θ-alumina, δ-alumina, and η-alumina.
  • From the viewpoint of more effectively suppressing the deterioration of the catalytic activity of the catalyst composition of the present invention, the content of the α-alumina in the carrier is preferably 90% by mass or more, more preferably 95% by mass or more, even more preferably 98% by mass or more, based on the mass of the carrier. The upper limit is 100% by mass.
  • The content of each element in the carrier can be measured by analyzing a sample obtained from the catalyst compositions of the present invention by energy dispersive X-ray spectroscopy (EDS) to obtain an element mapping, and performing EDS elemental analysis on designated particles in the obtained element mapping. Specifically, the content of each element in the designated particles can be measured by qualitatively identifying (color-coding) the carrier particles and other particles by elemental mapping and performing composition analysis (elemental analysis) on the designated particles. The content of alumina in the carrier can be calculated as an amount of Al in terms of Al2O3, based on the content of Al in the carrier. The crystal form of alumina in the carrier can be determined by X-ray diffraction (XRD).
  • The content of the carrier in the catalyst composition of the present invention can be appropriately adjusted. From the viewpoint of more effectively suppressing the deterioration of the catalytic activity of the catalyst composition of the present invention, the content of the carrier in the catalyst composition of the present invention is adjusted so that the content of α-alumina derived from the carrier is preferably 70% by mass or more and 95% by mass or less, more preferably 75% by mass or more and 95% by mass or less, and even more preferably 80% by mass or more and 95% by mass or less, based on the mass of catalyst composition of the present invention.
  • In a case where a composition of raw materials used in the production of the catalyst composition of the present invention is determined, the content of α-alumina in the catalyst composition of the present invention can be calculated from the composition of the raw materials used in the production of the catalyst composition of the present invention.
  • In a case where the composition of the raw materials used in the production of the catalyst composition of the present invention is not determined, the content of α-alumina in the catalyst composition of the present invention can be measured using a conventional method such as scanning electron microscopy-energy dispersive X-ray spectroscopy (SEM-EDX), X-ray fluorescence analysis (XRF), and inductively coupled plasma atomic emission spectrometry (ICP-AES). Specifically, the method is as follows.
  • First, a sample obtained from the catalyst composition of the present invention is analyzed by XRF or ICP-AES to identify 20 metal elements in descending order, from higher content to lower content. The 20 identified metal elements include Al.
  • The sample is then analyzed by SEM-EDX. In SEM-EDX, the 20 metal elements identified above are targeted for analysis. For each of 10 visual fields of the SEM, the total mole % of the 20 metal elements is set to 100 mole % to analyze the mole % of each metal element. The content of Al in the sample in terms of Al2O3 is calculated from the average value of the mole % of Al in the 10 visual fields.
  • The crystal form of alumina in the sample can be determined by X-ray diffraction (XRD).
    • <Supported Components>
  • The catalyst composition of the present invention includes supported components supported on the carrier.
  • The expression “a component is supported on the carrier” means a state in which the component is physically or chemically adsorbed or retained on the outer surfaces or inner surfaces of the pores of the carrier. The fact that the component is supported on the carrier can be confirmed using, for example, a scanning electron microscope-energy dispersive X-ray analyzer (SEM-EDX). Specifically, in the elemental mapping obtained using SEM-EDX or the like, when the component and the carrier are present in the same region, it can be determined that the component is supported on the carrier.
  • The supported components include at least one platinum group element, a Ce oxide, and a Zr oxide. In other words, the catalyst composition of the present invention includes at least one platinum group element supported on the carrier, a Ce oxide supported on the carrier, and a Zr oxide supported on the carrier. The platinum group element is a catalytically active component, while the Ce oxide and the Zr oxide are cocatalyst components.
  • In a case where the Ce oxide coexists with the Zr oxide, sintering of the Ce oxide and sintering of the platinum group element associated with the sintering of the Ce oxide and/or embedding of the platinum group element associated with the sintering of the Ce oxide are less likely to occur than in a case where the Ce oxide alone exists. Therefore, even when the catalyst composition of the present invention is exposed to a high temperature, the catalytic activity of the catalyst composition is unlikely to deteriorate.
  • The at least one platinum group element can be selected from the group of platinum group elements consisting of Pt, Pd, Rh, Ru, Os, and Ir. From the viewpoint of more effectively expressing catalytic activity, the at least one platinum group element preferably includes Pt and Rh.
  • From the viewpoint of achieving a good balance between catalytic activity and production cost, the content of the platinum group element in terms of metal is preferably 0.1% by mass or more and 2.0% by mass or less, more preferably 0.3% by mass or more and 1.5% by mass or less, and even more preferably 0.5% by mass or more and 1.0% by mass or less, based on the mass of the catalyst composition of the present invention. The term “the content of the platinum group element in terms of metal” means the content of one platinum group element in terms of metal if the catalyst composition of the present invention contains the one platinum group element, and the total content of two or more platinum group elements in terms of metal when the catalyst composition of the present invention contains the two or more platinum group elements. The content of the platinum group element in the catalyst composition of the present invention can be calculated or measured in the same manner as the content of α-alumina in the catalyst composition of the present invention.
  • The platinum group element is supported on the carrier in a form capable of functioning as a catalytically-active component, for example, in the form of a metal composed of the platinum group element, an alloy containing the platinum group element, a compound containing the platinum group element (such as an oxide of the platinum group element), or the like. The catalytically-active component is, for example, particulate.
  • The Ce oxide is composed of a Ce element and an O element. Although a stoichiometric composition of the Ce oxide is represented by CeO2, the Ce oxide may have a composition that deviates from the stoichiometric composition (non-stoichiometric composition). The composition of the Ce oxide contained in the catalyst composition of the present invention may be stoichiometric composition or non-stoichiometric composition (e.g., CeO1.8 and CeO1.9). The composition of the Ce oxide is preferably represented by CeOx (x=1.50 to 2.00), more preferably by CeOx (x=1.75 to 2.00), and even more preferably by CeOx (x=1.80 to 2.00). The catalyst composition of the present invention may contain one type of Ce oxide, or two or more types of Ce oxides.
  • The Zr oxide is composed of a Zr element and an O element. Although a stoichiometric composition of the Zr oxide is represented by ZrO2, the Zr oxide may have a composition that deviates from the stoichiometric composition (non-stoichiometric composition). The composition of the Zr oxide contained in the catalyst composition of the present invention may be stoichiometric composition or non-stoichiometric composition (e.g., ZrO1.8 and ZrO1.9). The composition of the Zr oxide is preferably represented by ZrOx (x=1.50 to 2.00), more preferably by ZrOx (x=1.75 to 2.00), and even more preferably by ZrOx (x=1.80 to 2.00). The catalyst composition of the present invention may contain one type of Zr oxide, or two or more types of Zr oxides.
  • The Ce oxide and the Zr oxide are, for example, particulate.
  • From the viewpoint of more effectively suppressing the sintering of the Ce oxide and the sintering of the platinum group element associated with the sintering of the Ce oxide and/or the embedding of the platinum group element associated with the sintering of the Ce oxide to more effectively suppressing the deterioration of the catalytic activity of the catalyst composition of the present invention, the content of the Ce oxide in the catalyst composition of the present invention in terms of CeO2 is preferably 8.5% by mass or more and 13.5% by mass or less, more preferably 9.0% by mass or more and 13.0% by mass or less, and even more preferably 9.5% by mass or more and 12.5% by mass or less, based on the mass of the catalyst composition of the present invention. The term “the content of the Ce oxide in terms of CeO2” means the content of one Ce oxide in terms of CeO2 when the catalyst composition of the present invention contains the one Ce oxide, and the total content of two or more Ce oxides in terms of CeO2 when the catalyst composition of the present invention contains the two or more Ce oxides. The content of the Ce oxide in the catalyst composition of the present invention in terms of CeO2 can be calculated or measured in the same manner as the content of α-alumina in the catalyst composition of the present invention.
  • From the viewpoint of more effectively suppressing the sintering of the Ce oxide and the sintering of the platinum group element associated with the sintering of the Ce oxide and/or the embedding of the platinum group element associated with the sintering of the Ce oxide to more effectively suppressing the deterioration of the catalytic activity of the catalyst composition of the present invention, the content of the Zr oxide in the catalyst composition of the present invention in terms of ZrO2 is preferably 0.3% by mass or more and 2.5% by mass or less, more preferably 0.4% by mass or more and 2.0% by mass or less, and even more preferably 0.5% by mass or more and 1.5% by mass or less, based on the mass of the catalyst composition of the present invention. The term “the content of the Zr oxide in terms of ZrO2” means the content of one Zr oxide in terms of ZrO2 when the catalyst composition of the present invention contains the one Zr oxide, and the total content of two or more Zr oxides in terms of ZrO2 when the catalyst composition of the present invention contains the two or more Zr oxides. The content of the Zr oxide in the catalyst composition of the present invention in terms of ZrO2 can be calculated or measured in the same manner as the content of α-alumina in the catalyst composition of the present invention.
  • From the viewpoint of more effectively suppressing the sintering of the Ce oxide and the sintering of the platinum group element associated with the sintering of the Ce oxide and/or the embedding of the platinum group element associated with the sintering of the Ce oxide to more effectively suppressing the deterioration of the catalytic activity of the catalyst composition of the present invention, the ratio of the Ce oxide in terms of CeO2 to the total content of the Ce oxide in terms of CeO2 and the Zr oxide in terms of ZrO2 is preferably 0.77 or more and 0.98 or less, more preferably 0.82 or more and 0.97 or less, and even more preferably 0.86 or more and 0.96 or less.
  • At least a part of the Ce oxide and at least a part of the Zr oxide are preferably present in the form of a composite oxide (a composite oxide containing Ce and Zr, hereinafter referred to as “Ce—Zr composite oxide”). The Ce—Zr composite oxide is, for example, particulate. In a case where the Ce oxide and the Zr oxide are present in the form of the Ce—Zr composite oxide, sintering of the Ce oxide and sintering of the platinum group element associated with the sintering of the Ce oxide and/or embedding of the platinum group element associated with the sintering of the Ce oxide are less likely to occur, compared to a case where the Ce oxide and the Zr oxide are present separately. Therefore, in the case where at least a part of the Ce oxide and at least a part of the Zr oxide are present in the form of the Ce—Zr composite oxide, the sintering of the Ce oxide and the sintering of the platinum group element associated with the sintering of the Ce oxide and/or the embedding of the platinum group element associated with the sintering of the Ce oxide are more effectively suppressed, thus more effectively suppressing the deterioration of the catalytic activity of the catalyst composition of the present invention.
  • The entire Ce oxide may be present in the form of the Ce—Zr composite oxide, and the entire Zr oxide may be present in the form of the Ce—Zr composite oxide.
  • In the Ce—Zr composite oxide, Ce, Zr, and O preferably form a solid solution phase. In addition to the solid solution phase, Ce, Zr, and O may form a single phase (Ce oxide phase and/or Zr oxide phase), which is a crystalline phase or an amorphous phase.
  • The presence of at least a part of the Ce oxide and at least a part of the Zr oxide in the form of the Ce—Zr composite oxide can be confirmed based on the fact that at least one peak derived from the Ce oxide has a peak top at 2θ=47.61° to 49° in an X-ray diffraction (XRD) pattern of a sample obtained from the catalyst composition of the present invention.
  • The XRD pattern can be obtained by performing XRD with CuKα using a sample obtained from the catalyst composition of the present invention and a commercially available X-ray diffraction device. Specific XRD conditions are as mentioned in Examples.
  • The catalyst composition of the present invention may include one or more other supported components supported on the carrier. Examples of such other components include oxides of rare earth metal elements other than Ce (e.g., Nd, La, Y, and Pr) and oxides of alkaline earth metal elements (e.g., Mg, Ca, Sr, and Ba). These oxides are, for example, particulate. At least a part of these oxides may form a composite oxide with the Ce oxide and/or the Zr oxide.
  • From the viewpoint of more effectively expressing the effects of the catalyst composition of the present invention, the total content of such other supported components is preferably 5% by mass or less, more preferably 3% by mass or less, and even more preferably 1% by mass or less, based on the mass of the catalyst composition of the present invention. The lower limit is zero. The content of such other supported components in the catalyst composition of the present invention can be calculated or measured in the same manner as the content of α-alumina in the catalyst composition of the present invention.
  • From the viewpoint of more effectively suppressing the deterioration of the catalytic activity of the catalyst composition of the present invention, the sum of the content of α-alumina derived from the carrier, the content of the Ce oxide supported on the carrier in terms of CeO2, and the content of the Zr oxide supported on the carrier in terms of ZrO2 is preferably 98.0% by mass or more and 99.9% by mass or less, more preferably 98.5% by mass or more and 99.7% by mass or less, and even more preferably 99.0% by mass or more and 99.5% by mass or less, based on the mass of the catalyst composition of the present invention.
    • <Method of Producing Catalyst Composition>
  • The catalyst composition of the present invention can be produced, for example, by mixing a solution containing a salt of a platinum group element, a solution containing a cerium salt, a solution containing a zirconium salt, and carrier particles each containing α-alumina, followed by drying and calcination. The calcined product may be pulverized as necessary. The salt of the platinum group element may be, for example, a nitrate, an ammine complex salt, a chloride or the like. The cerium salt may be, for example, a nitrate, an acetate or the like. The zirconium salt may be, for example, a nitrate, an acetate or the like. The solvents contained in the solution containing the salt of the platinum group element, the solution containing the cerium salt, and the solution containing the zirconium salt are each, for example, water (such as ion exchanged water). The solution containing the salt of the platinum group element, the solution containing the cerium salt, and the solution containing the zirconium salt may each contain an organic solvent such as alcohol. The drying temperature is, for example, 70° C. or higher and 150° C. or lower. The calcination temperature is, for example, 400° C. or higher and 700° C. or lower. The calcination time is, for example, 1 hour or more and 10 hours or less. The calcination can be carried out, for example, in an air atmosphere.
  • The carrier particles each containing α-alumina used in the production of the catalyst composition of the present invention preferably have the following physical properties.
  • The BET specific surface area of the carrier particles is preferably 1 m2/g or more and 20 m2/g or less, and more preferably 2 m2/g or more and 10 m2/g or less.
  • The BET specific surface area is measured according to JIS R1626, “Measuring methods for the specific surface area of fine ceramic powders by gas adsorption using the BET method,” “6.2 Flow method,” “(3.5) Single-point method.” In this method, a nitrogen-helium gas mixture containing 30% by volume of nitrogen as an adsorption gas and 70% by volume of helium as a carrier gas is used as a gas. For example, BELSORP-MR6 manufactured by MicrotracBEL Corp. is used as a measurement device.
  • The pore volume (total pore volume in the range of a pore diameter of 3 nm or more and 500 μm or less) of the carrier particles is preferably 0.3 cm3/g or more and 0.6 cm3/g or less, and more preferably 0.4 cm3/g or more and 0.5 cm3/g or less.
  • The pore volume is measured by mercury porosimetry using a mercury porosimeter. The mercury porosimetry is performed in accordance with JIS R 1655:2003. For example, AutoPore IV 9520, manufactured by SHIMADZU CORPORATION, is used as a measuring device.
  • The average particle size of the carrier particles is preferably 1.0 mm or more and 5.0 mm or less, and more preferably 2.0 mm or more and 4.0 mm or less.
  • A method of measuring the average particle size of the carrier particles is as follows. The carrier particles are observed using an optical microscope, and unidirectional particle diameters (Feret diameters) of 100 carrier particles arbitrarily selected from the visual field are measured to define an average value as the average particle size of the carrier particles.
  • The packing density (tap density) of the carrier particles is preferably 0.70 g/cm3 or more and 1.00 g/cm3 or less, and more preferably 0.80 g/cm3 or more and 0.90 g/cm3 or less.
  • A method of measuring the packing density (tap density) of the carrier particles is as follows. 30 g of carrier particles is put in a 150-ml glass measuring cylinder and tapped 350 times in a stroke of 60 mm with a shaking specific gravity meter (KRS-409, manufactured by Kuramochi Kagaku Kikai Seisakusho K.K), and then the packing density (tap density) is measured.
    • <<Fuel Cell System>>
  • A fuel cell system 100 according to one embodiment of the invention is described below based on FIG. 1 . Two or more of embodiments described below can be used in combination, and the combination of two or more embodiments is also encompassed by the present invention.
  • A fuel cell system 100 can be used for various applications, including stationary as well as automotive use and the like.
  • As illustrated in FIG. 1 , the fuel cell system 100 includes a processing unit 110 and a control unit 111 that controls operation of the processing unit 110.
  • The various processes carried out by the processing unit 110 are described later.
  • The control unit 111 is, for example, a computer and includes a main control unit and a storage unit. The main control unit is, for example, a CPU (central processing unit), and controls the operation of the processing unit 110 by reading and executing programs, data, and the like stored in the storage unit. The storage unit is composed of, for example, a RAM (Random Access Memory), a ROM (Read Only Memory), a hard disk, or other storage devices, and stores programs, data, and the like that control processes executed by the processing unit 110.
  • As illustrated in FIG. 1 , the processing unit 110 in the fuel cell system 100 includes a hydrocarbon partial oxidizer 12, a fuel cell 16, a raw material supplying unit 17, and an oxidant gas supplying unit 19.
  • As illustrated in FIG. 1 , the processing unit 110 in the fuel cell system 100 may optionally include a mixer 13, a steam reformer 14, a shift reactor 15, and a steam supplying unit 18.
  • The raw material supplying unit 17 supplies a raw material gas G1 containing a hydrocarbon to the hydrocarbon partial oxidizer 12. The raw material gas G1 includes one or more hydrocarbon-containing materials selected from, for example, city gas, natural gas, LPG, naphtha, gasoline, kerosene, and light oil. The raw material gas G1 may contain hydrogen, water, carbon dioxide, carbon monoxide, nitrogen, oxygen, and the like. In one embodiment, the raw material gas G1 contains air. The air may be mixed with a hydrocarbon in the raw material supplying unit 17, or may be mixed with the hydrocarbon on the way that the hydrocarbon is supplied from the raw material supplying unit 17 to the hydrocarbon partial oxidizer 12.
  • In one embodiment, the raw material supplying unit 17 includes a tank for storing the raw material gas G1, a supply pipe for supplying the raw material gas G1 in the tank to the hydrocarbon partial oxidizer 12, and a pump provided in the supply pipe, and supplies the raw material gas G1 in the tank to the hydrocarbon partial oxidizer 12 through the supply pipe by using sucking and discharging forces of the pump.
  • The raw material supplying unit 17 may include a desulfurizer for desulfurizing the raw material gas G1. In one embodiment, the desulfurizer includes a container and a desulfurizing agent contained within the container. As the desulfurizing agent, a known agent can be used.
  • The O2/C (ratio of the molar amount of oxygen molecules to the molar amount of carbon atoms contained in the hydrocarbon) in the raw material gas G1 can be appropriately set depending on a desired yield of hydrogen, characteristics of the fuel cell system, reaction conditions, and the like.
  • The hydrocarbon partial oxidizer 12 includes the catalyst composition of the present invention. In one embodiment, the hydrocarbon partial oxidizer 12 includes a container and the catalyst composition of the invention contained within the container.
  • The raw material gas G1 supplied to the hydrocarbon partial oxidizer 12 is brought into contact with the catalyst composition of the present invention, and a hydrocarbon in the raw material gas G1 is partially oxidized to produce a reformed gas G2 containing hydrogen and carbon monoxide.
  • When the hydrocarbon is CnHm, the partial oxidation reaction is represented by the following equation.

  • Partial oxidation reaction: CnHm +n/2O2 →m/2H2 +nCO
  • Conditions of the partial oxidation reaction in the hydrocarbon partial oxidizer 12 are not particularly limited as long as the partial oxidation reaction can proceed. The temperature is preferably 100° C. or higher and 1,000° C. or lower, more preferably 200° C. or higher and 800° C. or lower, and even more preferably 300° C. or higher and 700° C. or lower.
  • In one embodiment, the reformed gas G2 produced in the hydrocarbon partial oxidizer 12 is supplied to the fuel cell 16. The reformed gas G2 is supplied to an anode electrode 161 side of the fuel cell 16. The fuel cell 16 generates electric power by electrochemical reaction between hydrogen in the reformed gas G2 and oxygen in an oxidant gas R supplied by the oxidant gas supplying unit 19.
  • Optionally, a mixer 13 may be provided. In a case where the mixer 13 is provided, the reformed gas G2 produced in the hydrocarbon partial oxidizer 12 is supplied to the mixer 13.
  • Optionally, a steam supplying unit 18 may be provided. The steam supplying unit 18 supplies steam W to the mixer 13. The steam supplying unit 18 may include a steam generating unit for generating the steam W from water. In one embodiment, the steam supplying unit 18 includes a tank for storing the steam W, a supply pipe for supplying the steam in the tank to the mixer 13, and a pump provided in the supply pipe, and supplies the steam W in the tank to the mixer 13 through the supply pipe by using sucking and discharging forces of the pump.
  • In the mixer 13, the reformed gas G2 and the steam W are mixed to generate a mixed gas G3 containing the reformed gas G2 and the steam W. The generated mixed gas G3 is supplied to the steam reformer 14.
  • Optionally, the steam reformer 14 may be provided. The steam reformer 14 includes a catalyst composition for steam reforming reaction. In one embodiment, the steam reformer 14 includes a container and the catalyst composition for steam reforming reaction contained within the container. As the catalyst composition for the steam reforming reaction, a known composition can be used.
  • The mixed gas G3 supplied to the steam reformer 14 is brought into contact with the catalyst composition for steam reforming reaction, and a hydrocarbon in the mixed gas G3 is steam-reformed to produce a reformed gas G4 containing hydrogen and carbon monoxide.
  • When the hydrocarbon is CnHm, the steam reforming reaction is represented by the following equation.

  • Steam reforming reaction: CnHm +nH2O→(m/2+n)H2 +nCO
  • As conditions of the steam reforming reaction in the steam reformer 14, known conditions can be applied.
  • In one embodiment, the reformed gas G4 produced in the steam reformer 14 is supplied to the fuel cell 16. The reformed gas G4 is supplied to an anode electrode 161 side of the fuel cell 16. The fuel cell 16 generates electric power by electrochemical reaction between hydrogen in the reformed gas G4 and oxygen in an oxidant gas R supplied by the oxidant gas supplying unit 19.
  • Optionally, a shift reactor 15 may be provided. In a case where the shift reactor 15 is provided, the reformed gas G4 produced in the steam reformer 14 is supplied to the shift reactor 15. The shift reactor 15 includes a catalyst composition for water-gas shift reaction. In one embodiment, the shift reactor 15 includes a container and the catalyst composition for water-gas shift reaction contained within the container. As the catalyst composition for water-gas shift reaction, a known composition can be used.
  • The reformed gas G4 supplied to the shift reactor 15 is brought into contact with the catalyst composition for water-gas shift reaction, and carbon monoxide and steam in the reformed gas G4 react to produce a fuel gas G5 containing hydrogen and carbon dioxide.
  • The water-gas shift reaction is represented by the following equation.

  • Water-gas shift reaction: CO+H2O→H2+CO2
  • As conditions of the water-gas shift reaction in the shift reactor 15, known conditions can be applied.
  • In one embodiment, the fuel gas G5 produced in the shift reactor 15 is supplied to the fuel cell 16. The fuel gas G5 is supplied to the anode electrode 161 side of the fuel cell 16. The fuel cell 16 generates electric power by electrochemical reaction between hydrogen in the fuel gas G5 and oxygen in an oxidant gas R supplied by the oxidant gas supplying unit 19.
  • The oxidant gas supplying unit 19 supplies an oxidant gas R to the fuel cell 16. The oxidant gas R is, for example, air. The oxidant gas R is supplied to a cathode electrode 162 side of the fuel cell 16. In one embodiment, the oxidant gas supplying unit 19 includes a tank for storing the oxidant gas R, a supply pipe for supplying the oxidant gas R in the tank to the fuel cell 16, and a pump provided in the supply pipe, and supplies the oxidant gas R in the tank to the fuel cell 16 through the supply pipe by using sucking and discharging forces of the pump.
  • As the fuel cell 16, a known fuel cell can be used. The fuel cell 16 is, for example, a solid oxide fuel cell (SOFC). A plurality of fuel cells 16 may be laminated to form a fuel cell stack.
  • The fuel cell 16 is, for example, an electrolyte/electrode assembly (MEA) in which the anode electrode 161 and the cathode electrode 162 are respectively provided on one surface and the other surface of an electrolyte 163 composed of an oxide ion conductor such as stabilized zirconia.
  • At the anode electrode 161, a reaction proceeds in which hydrogen reacts with oxide ions to form water and release electrons, while at the cathode electrode 162, a reaction proceeds in which oxygen gains electrons to become oxide ions. An electric load (not shown) may be connected electrically to the anode electrode 161 and the cathode electrode 162.
    • EXAMPLES Example 1
  • Under an environment of 120° C., 100 g of spherical α-alumina pellets (specific surface area: about 4 m2/g, pore volume: about 0.43 cm3/g, packing density: about 0.86 g/cm3, average particle size: about 2.5 mm) were allowed to stand and dried for 5 hours to give dried alumina pellets.
  • A platinum nitrate solution and a rhodium nitrate solution were each weighed so that the sum of the content of Pt in terms of metal and the content of Rh in terms of metal was 0.5% by mass or more and 1.0% by mass or less, based on the mass of the final product, Pt—Rh-ceria-zirconia-supporting calcined alumina pellet. A cerium nitrate solution and a zirconium nitrate solution were each weighed so that the content of the Ce oxide in terms of CeO2 and the content of the Zr oxide in terms of ZrO2 were as shown in Table 1, based on the mass of the final product, Pt—Rh-ceria-zirconia-supporting calcined alumina pellet. The solutions were mixed and stirred for 10 minutes to give a mixed solution. The obtained mixed solution was charged into the dried alumina pellets and stirred for 10 minutes to allow the alumina pellets to absorb the mixed solution. The content of the dried alumina pellets charged was adjusted so that the content of solid matter of the alumina pellets absorbed with the mixed solution was 100 g in total. The alumina pellets having absorbed the mixed solution were dried under an environment of 120° C. until no weight change was observed to give Pt—Rh-cerium-zirconium-supporting dried alumina pellets.
  • The obtained Pt—Rh-cerium-zirconium-supporting dried alumina pellets were calcined at 500° C. for 3 hours to give Pt—Rh-ceria-zirconia-supporting calcined alumina pellets. The composition of the obtained Pt—Rh-ceria-zirconia-supporting calcined alumina pellets is shown in Table 1. Note that in Table 1, “% by mass” in Example 1 is based on the mass of the Pt—Rh-ceria-zirconia-supporting calcined alumina pellet.
  • An X-ray diffraction (XRD) pattern of the Pt—Rh-ceria-zirconia-supporting calcined alumina pellets was measured using X-ray diffraction (XRD). XRD was performed using an X-ray diffractometer under the following conditions: X-ray source: CuKα, operating axis: 2θ/θ, measuring method: continuous, counting unit: cps, starting angle: 5°, ending angle: 80°, step width: 0.02°, scanning speed: 10.0°/min, voltage: 40 kV, and current: 15 mA.
  • In the measured X-ray diffraction pattern, there was a peak derived from a Ce oxide having a peak top at 2θ=47.61° to 49° (specifically, 2θ=47.68°).
    • Comparative Example 1
  • The platinum nitrate solution and the rhodium nitrate solution were weighed so that the content (% by mass) of Pt in terms of metal and the content (% by mass) of Rh in terms of metal were each the same as in Example 1, based on the mass of the final product, Pt—Rh-ceria-supporting calcined alumina pellet. The cerium nitrate solution was weighed so that the content of the Ce oxide in terms of CeO2 was as shown in Table 1, based on the mass of the final product, Pt—Rh-ceria-supporting calcined alumina pellet. The same operation as in Example 1 was carried out to give Pt—Rh-cerium-supporting dried alumina pellets, except that the solutions were mixed and stirred for 10 minutes and a mixed solution was obtained (a zirconium nitrate solution was not used). The obtained Pt—Rh-cerium-supporting dried alumina pellets were calcined at 500° C. for 3 hours to give Pt—Rh-ceria-supporting calcined alumina pellets. The composition of the obtained Pt—Rh-ceria-supporting calcined alumina pellets is shown in Table 1. Note that in Table 1, “% by mass” in Comparative Example 1 is based on the mass of the Pt—Rh-ceria-supporting calcined alumina pellet.
  • An X-ray diffraction (XRD) pattern of the Pt—Rh-ceria-supporting calcined alumina pellets was obtained using X-ray diffraction (XRD). XRD was performed in the same manner as in Example 1. In the measured X-ray diffraction pattern, there was a peak derived from a Ce oxide having a peak top at 2θ=47.60°, but there was no peak derived from a Ce oxide having a peak top at 2θ=47.61° to 49°.
    • Comparative Example 2
  • The same operation as in Example 1 was carried out to give Pt—Rh-cerium-zirconium-supporting dried alumina pellets, except that under an environment of 120° C., 100 g of spherical γ-alumina pellets (specific surface area: about 210 m2/g, pore volume: about 0.43 cm3/g, packing density: about 0.85 g/cm3, average particle size: about 2.5 mm) were allowed to stand and dried for 5 hours, and dried alumina pellets were obtained. Note that the content (% by mass) of Pt in terms of metal and the content (% by mass) of Rh in terms of metal were each the same as in Example 1, based on the mass of the final product, Pt—Rh-ceria-zirconia-supporting calcined alumina pellet. The obtained Pt—Rh-cerium-zirconium-supporting dried alumina pellets were calcined at 500° C. for 3 hours to give Pt—Rh-ceria-zirconia-supporting calcined alumina pellets. The composition of the obtained Pt—Rh-ceria-zirconia-supporting calcined alumina pellets is shown in Table 1. Note that in Table 1, “% by mass” in Comparative Example 2 is based on the mass of the Pt—Rh-ceria-zirconia-supporting calcined alumina pellet.
  • An X-ray diffraction (XRD) pattern of the Pt—Rh-ceria-zirconia-supporting calcined alumina pellets were obtained using X-ray diffraction (XRD). XRD was performed in the same manner as in Example 1. In the measured X-ray diffraction pattern, there was a peak derived from a Ce oxide having a peak top at 2θ=47.54°, but there was no peak derived from a Ce oxide having a peak top at 2θ=47.61° to 49°.
  • TABLE 1
    Contents of
    supported
    Carrier components
    Content (% by mass)
    Type (% by mass) CeO2 ZrO2
    Example 1 α-alumina 87 11 1
    Comparative α-alumina 87 12 —
    Example 1
    Comparative γ-alumina 87 11 1
    Example 2
    • Test Example 1 (1) Accelerated Aging Treatment
  • The Pt—Rh-ceria-zirconia-supporting calcined alumina pellets obtained in Example 1 were installed in a tubular furnace, and a simulated fuel gas containing air and hydrocarbon was circulated. In the simulated fuel gas, the ratio of the molar amount of oxygen molecules derived from the air to the molar amount of carbon atoms derived from the hydrocarbon (O2/C ratio) was adjusted to be 0.5. The temperature of the tubular furnace was increased to 1,000° C. at a temperature increasing rate of 5° C./min while the simulated fuel gas was circulated, and the Pt—Rh-ceria-zirconia-supporting calcined alumina pellets obtained in Example 1 were treated at 1,000° C. for 24 hours to prepare an aging-treated sample.
  • The Pt—Rh-ceria-supporting calcined alumina pellets obtained in Comparative Example 1 and the Pt—Rh-ceria-zirconia-supporting calcined alumina pellets obtained in Comparative Example 2 were also subjected to the same accelerated aging treatment as described above to prepare aging-treated samples.
    • (2) Ignition Temperature Measurement
  • The evaluation device illustrated in FIG. 2 was used to measure the ignition temperature of the aging-treated samples.
  • In the evaluation device illustrated in FIG. 2 , the flow rates of fuel gas (city gas) supplied from a cylinder 1 and air supplied from a cylinder 3 are adjusted by a gas mass flow controller 2 and a gas mass flow controller 4, respectively. The fuel gas supplied from the cylinder 1 and the air supplied from the cylinder 3 are mixed in a mixing unit 5 and transferred to a partial oxidation catalyst 7 contained within a stainless steel container in an electric furnace 6, and the gas partially oxidized by the partial oxidation catalyst 7 is discharged through a bubbler 8. Note that each of the aging-treated samples obtained in (1) above were used as the partial oxidation catalyst 7.
  • The ignition temperature and the temperature after heating were measured according to the following procedure. Note that the amount of the partial oxidation catalyst 7 in the stainless steel container in the electric furnace 6 was adjusted to a volume of 1.5 cm3, and the flow rates of the fuel gas and air supplied to the partial oxidation catalyst 7 were adjusted so that the space velocity (SV) divided by the catalyst volume was about 30,000 h−1, and the ratio of the molar amount of oxygen molecules in the supplied air to the molar amount of carbon atoms in the supplied fuel gas (O2/C ratio) was 0.5.
  • (a) The temperature of the electric furnace was increased until the temperature of the furnace, as measured by a thermocouple 9, reached 200° C.
  • (b) The setting temperature of the electric furnace was increased by 10° C., the temperature of the partial oxidation catalyst 7 was measured by a thermocouple 10, and the temperature of an inlet gas was measured by a thermocouple 11 located in front of the partial oxidation catalyst 7.
  • (c) In a case where the difference between the temperature of the inlet gas and the temperature of the partial oxidation catalyst 7 after the stop of the temperature rise was less than 20° C., it was determined that ignition did not occur in the temperature range, and the procedure of (b) was performed again. Herein, the stop of the temperature rise indicates that a change in the temperature of the partial oxidation catalyst 7 is 1° C./min or less.
  • (d) In a case where the difference between the temperature of the inlet gas and the temperature of the partial oxidation catalyst 7 after the stop of the temperature rise was 20° C. or more, it was determined that ignition has occurred, and the temperature of the partial oxidation catalyst 7 before the start of the temperature rise was defined as the ignition temperature while the temperature after the stop of the temperature rise was defined as the temperature after heating. Table 2 shows results.
  • TABLE 2
    Ignition Temperature after
    temperature (° C.) heating (° C.)
    Example 1 500 590
    Comparative 535 600
    Example 1
    Comparative 585 610
    Example 2
  • In the aging-treated sample of Example 1, even when exposed to a high temperature, a state in which the reaction gas easily reaches the supported components supported deep into the pores of the carrier was maintained by using α-alumina as the carrier. Furthermore, because of the inclusion of the Zr oxide, the effects of preventing the sintering of the platinum group element associated with the sintering of the Ce oxide and/or the embedding of the platinum group element associated with the sintering of the Ce oxide were preferably exhibited. As a result, the activity of the catalyst did not decrease, the state in which the partial oxidation reaction easily occurred was maintained, and showed the low ignition temperature.
  • In the aging-treated sample of Comparative Example 1, because the Zr oxide was not contained, the effects of preventing the sintering of the Ce oxide and the sintering of the platinum group element associated with the sintering of the Ce oxide and/or the embedding of the platinum group element associated with the sintering of the Ce oxide were not exhibited. As a result, the activity of the catalyst decreased, the partial oxidation reaction was less likely to occur, and ignition occurred at a temperature higher than that in Example 1.
  • In the aging-treated sample of Comparative Example 2, because γ-alumina was used as the carrier, the embedding of the platinum group element supported on the outer surface thereof and the blockage of the pores of the γ-alumina occurred and thus caused the reaction gas to hardly reach the supported components. As a result, the activity of the catalyst decreased, the partial oxidation reaction was less likely to occur, and ignition occurred at a temperature higher than that in Example 1.
    • REFERENCE SIGNS LIST
      • 100 Fuel cell system
      • 110 Processing unit
      • 111 Control unit
      • 12 Hydrocarbon partial oxidizer
      • 13 Mixer
      • 14 Steam reformer
      • 15 Shift reactor
      • 16 Fuel cell
      • 17 Raw material supplying unit
      • 18 Steam supplying unit
      • 19 Oxidant gas supplying unit

Claims (9)

What is claimed is:
1. A catalyst composition that partially oxidizes a hydrocarbon to produce hydrogen and carbon monoxide, the catalyst composition comprising: a carrier that comprises α-alumina; and supported components that are supported on the carrier,
wherein the supported components comprise at least one platinum group element, a Ce oxide, and a Zr oxide.
2. The catalyst composition according to claim 1, wherein a content of the α-alumina is 70% by mass or more and 95% by mass or less, based on a mass of the catalyst composition.
3. The catalyst composition according to claim 1, wherein a content of the Ce oxide in terms of CeO2 is 8.5% by mass or more and 13.5% by mass or less, based on a mass of the catalyst composition.
4. The catalyst composition according to claim 1, wherein a content of the Zr oxide in terms of ZrO2 is 0.3% by mass or more and 2.5% by mass or less, based on a mass of the catalyst composition.
5. The catalyst composition according to claim 1, wherein at least a part of the Ce oxide and at least a part of the Zr oxide are present in a form of a composite oxide.
6. The catalyst composition according to claim 5, wherein in an X-ray diffraction pattern, at least one of peaks derived from the Ce oxide has a peak top at 2θ=47.61° to 49°.
7. The catalyst composition according to claim 1, wherein the at least one platinum group element comprises Pt and Rh.
8. A hydrocarbon partial oxidizer that partially oxidizes a hydrocarbon to produce hydrogen and carbon monoxide, the hydrocarbon partial oxidizer comprising the catalyst composition according to claim 1.
9. A fuel cell system comprising: the hydrocarbon partial oxidizer according to claim 8; and a fuel cell that generates electric power by a reaction between the hydrogen produced in the hydrocarbon partial oxidizer and an oxidant gas.
US18/087,920 2021-12-24 2022-12-23 Catalyst composition, hydrocarbon partial oxidizer, and fuel cell system Abandoned US20230201806A1 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
JP2021-211477 2021-12-24
JP2021211477A JP2023095527A (en) 2021-12-24 2021-12-24 Catalyst composition, hydrocarbon partial oxidizer and fuel cell system

Publications (1)

Publication Number Publication Date
US20230201806A1 true US20230201806A1 (en) 2023-06-29

Family

ID=86898754

Family Applications (1)

Application Number Title Priority Date Filing Date
US18/087,920 Abandoned US20230201806A1 (en) 2021-12-24 2022-12-23 Catalyst composition, hydrocarbon partial oxidizer, and fuel cell system

Country Status (2)

Country Link
US (1) US20230201806A1 (en)
JP (1) JP2023095527A (en)

Also Published As

Publication number Publication date
JP2023095527A (en) 2023-07-06

Similar Documents

Publication Publication Date Title
Bonura et al. Ceria–gadolinia supported NiCu catalyst: A suitable system for dry reforming of biogas to feed a solid oxide fuel cell (SOFC)
JP2006346598A (en) Steam reforming catalyst
US20130071318A1 (en) Fuel reformer, selective co methanation method, selective co methanation catalyst, and process for producing the same
Sadykov et al. Structured nanocomposite catalysts of biofuels transformation into syngas and hydrogen: Design and performance
Qihai et al. Hydrogen production by steam reforming of ethanol over copper doped Ni/CeO2 catalysts
Kroner et al. Structural Characterization of Alumina‐Supported Rh Catalysts: Effects of Ceriation and Zirconiation by using Metal–Organic Precursors
US20120201733A1 (en) Hydrocarbon-decomposing porous catalyst body and process for producing the same, process for producing hydrogen-containing mixed reformed gas from hydrocarbons, and fuel cell system
SG177851A1 (en) Method for forming a catalyst comprising catalytic nanoparticles and a catalyst support
US20110065017A1 (en) Catalyst materials and methods for reforming hydrocarbon fuels
Kosinski et al. Methanol reforming by nanostructured Pd/Sm-doped ceria catalysts
Ploner et al. The sol–gel autocombustion as a route towards highly CO 2-selective, active and long-term stable Cu/ZrO 2 methanol steam reforming catalysts
Oh et al. Negative Effects of Dopants on Copper–Ceria Catalysts for CO Preferential Oxidation Under the Presence of CO 2 and H 2 O
Sadykov et al. Design and characterization of nanocomposite catalysts for biofuel conversion into syngas and hydrogen in structured reactors and membranes
JP2012061398A (en) Catalyst for producing hydrogen, method for manufacturing the catalyst, and method for producing hydrogen by using the catalyst
Chen et al. Preparation, characterization and catalytic performance of high stability of LaCoO3@ CuO composite with core-shell structure for methanol steam reforming
US20230201806A1 (en) Catalyst composition, hydrocarbon partial oxidizer, and fuel cell system
JP2012210620A (en) Reforming catalyst for producing hydrogen, hydrogen producing apparatus using the catalyst and fuel cell system
US20200094227A1 (en) Catalyst for the methanation of syngas and producer gas
Dasireddy et al. Heterogeneous Cu–Fe oxide catalysts for preferential CO oxidation (PROX) in H 2-rich process streams
Jennings et al. Measurement and Characterization of a High-Temperature, Coke-Resistant Bi-functional Ni/BZY15 Water-Gas-Shift Catalyst Under Steam-Reforming Conditions
Matsumura et al. Deterioration mechanism of direct internal reforming catalyst
Smirnova et al. Design and testing of structured catalysts for internal reforming of CH4 in intermediate temperature solid oxide fuel cells (IT SOFC)
JP2015224141A (en) Reformer, method for producing hydrogen, apparatus for producing hydrogen, and fuel cell system
CN112449615B (en) Steam reforming catalyst
Sundararajan et al. Cooperative synergy in nanoscale ceria-based systems

Legal Events

Date Code Title Description
AS Assignment

Owner name: HONDA MOTOR CO., LTD., JAPAN

Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNORS:SAWADA, JUN;ISHII, WATARU;KURASHINA, DAISUKE;AND OTHERS;SIGNING DATES FROM 20221116 TO 20221212;REEL/FRAME:062280/0806

Owner name: MITSUI MINING & SMELTING CO., LTD., JAPAN

Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNORS:SAWADA, JUN;ISHII, WATARU;KURASHINA, DAISUKE;AND OTHERS;SIGNING DATES FROM 20221116 TO 20221212;REEL/FRAME:062280/0806

STPP Information on status: patent application and granting procedure in general

Free format text: DOCKETED NEW CASE - READY FOR EXAMINATION

STPP Information on status: patent application and granting procedure in general

Free format text: NON FINAL ACTION MAILED

STCB Information on status: application discontinuation

Free format text: ABANDONED -- FAILURE TO RESPOND TO AN OFFICE ACTION